Soybean variety

ABSTRACT

The present invention is directed in part to soybean variety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 breeding and development. The present invention particularly relates to soybean variety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 and its seed, cells, germplasm, plant parts, and progeny, and methods of using AR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104, e.g., in a breeding program.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to U.S. Provisional Application No.62/971,253, filed Feb. 7, 2020, the contents of which are incorporatedherein by reference.

THE FIELD OF THE INVENTION

The present invention is in the field of soybean cultivar breeding anddevelopment.

The present invention particularly relates to the soybean cultivarAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 and its seed, cells, germplasm, plant parts, and progeny, andits use in a breeding program.

BACKGROUND OF THE INVENTION

Soybean Glycine max (L) is an important oil seed crop and a valuablefield crop. However, it began as a wild plant. This plant and a numberof other plants have been developed into valuable agricultural cropsthrough years of breeding and development. The pace of the developmentof soybeans, into an animal foodstuff and as an oil seed hasdramatically increased in the last one hundred years. Planned programsof soybean breeding have increased the growth, yield and environmentalhardiness of the soybean germplasm.

Due to the sexual reproduction traits of the soybean, the plant isbasically self-pollinating. A self-pollinating plant permits pollen fromone flower to be transferred to the same or another flower of the sameplant. Cross-pollination occurs when the flower is pollinated withpollen from a different plant; however, soybean cross-pollination is arare occurrence in nature.

Thus the growth and development of new soybean germplasm requiresintervention by the breeder into the pollination of the soybean. Thebreeders' methods of intervening depends on the type of trait that isbeing bred. Soybeans are developed for a number of different types oftraits including morphology (form and structure), phenotypiccharacteristics, and for traits like growth, day length, relativematurity, temperature requirements, initiation date of floral orreproductive development, fatty acid content, insect resistance, diseaseresistance, nematode resistance, fungal resistance, herbicideresistance, tolerance to various environmental factors like drought,heat, wet, cold, wind, adverse soil condition and also for yield. Thegenetic complexity of the trait often drives the selection of thebreeding method.

Due to the number of genes within each chromosome, millions of geneticcombinations exist in the breeders' experimental soybean material. Thisgenetic diversity is so vast that a breeder cannot produce the same twocultivars twice using the exact same starting parental material. Thus,developing a single variety of useful commercial soybean germplasm ishighly unpredictable, and requires intensive research and development.

The development of new soybeans comes through breeding techniques, suchas: recurrent selection, mass selections, backcrossing, single seeddescent and multiple seed procedure. Additionally, marker assistedbreeding allows more accurate movement of desired alleles or evenspecific genes or sections of chromosomes to be moved within thegermplasm that the breeder is developing. RFLP, RAPD, AFLP, SSR, SNP,SCAR, and isozymes are some of the forms of markers that can be employedin breeding soybeans or in moving traits into soybean germplasm. Otherbreeding methods are known and are described in various plant breedingor soybean textbooks.

When a soybean variety is being employed to develop a new soybeanvariety or an improved variety, the selection methods may includebackcrossing, pedigree breeding, recurrent selection, marker assistedselection, modified selection and mass selection or a combination ofthese methods. The efficiency of the breeding procedure along with thegoal of the breeding are the main factors for determining whichselection techniques are employed. A breeder continuously evaluates thesuccess of the breeding program and therefore the efficiency of anybreeding procedures. The success is usually measured by yield increase,commercial appeal and environmental adaptability of the developedgermplasm.

The development of new soybean cultivars most often requires thedevelopment of hybrid crosses (some exceptions being initial developmentof mutants directly through the use of the mutating agent, certainmaterials introgressed by markers, or transformants made directlythrough transformation methods) and the selection of progeny. Hybridscan be achieved by manual manipulation of the sexual organs of thesoybean or by the use of male sterility systems. Breeders often try toidentify true hybrids by a readily identifiable trait or the visualdifferences between inbred and hybrid material. These heterozygoushybrids are then selected and repeatedly selfed and reselected to formnew homozygous soybean lines.

Mass and recurrent selection can be used to improve populations. Severalparents are intercrossed and plants are selected based on selectedcharacteristics like superior yield or excellent progeny resistance.Outcrossing to a number of different parents creates fairly heterozygousbreeding populations.

Pedigree breeding is commonly used with two parents that possessfavorable, complementary traits. The parents are crossed to form a F1hybrid. The progeny of the F1 hybrid is selected and the best individualF2s are selected; this selection process is repeated in the F3 and F4generations. The inbreeding is carried forward and at approximatelyF5-F7 the best lines are selected and tested in the development stagefor potential usefulness in a selected geographic area.

In backcross breeding a genetic allele or loci is often transferred intoa desirable homozygous recurrent parent. The trait from the donor parentis tracked into the recurrent parent. The resultant plant is bred to beessentially the same as the recurrent parent, with the same physiologyand morphological characteristics as the recurrent part, with the newdesired allele or loci.

The single-seed descent method involves use of a segregating plantpopulation for harvest of one seed per plant. Each seed sample isplanted and the next generation is formed. When the F2 lines areadvanced to approximately F6 or so, each plant will be derived from adifferent F2. The population will decline due to failure of some seeds,so not all F2 plants will be represented in the progeny.

New varieties must be tested thoroughly to compare their developmentwith commercially available soybeans. This testing usually requires atleast two years and up to six years of comparisons with other commercialsoybeans. Varieties that lack the entire desirable package of traits canbe used as parents in new populations for further selection or aresimply discarded. The breeding and associated testing process is 8 to 12years' of work prior to development of a new variety. Thousands ofvarietal lines are produced but only a few lines are selected in eachstep of the process. Thus the breeding system is like a funnel withnumerous lines and selections in the first few years and fewer and fewerlines in the middle years until one line is selected for the finaldevelopment testing.

The selected line or variety will be evaluated for its growth,development and yield. These traits of a soybean are a result of thevariety's genetic potential interacting with its environment. Allvarieties have a maximum yield potential that is predetermined by itsgenetics. This hypothetical potential for yield is only obtained whenthe environmental conditions are near perfect. Since perfect growthconditions do not exist, field experimentation is necessary to providethe environmental influence and to measure its effect on the developmentand yield of the soybean. The breeder attempts to select for an elevatedsoybean yield potential under a number of different environmentalconditions.

Selecting for good soybean yield potential in different environmentalconditions is a process that requires planning based on the analysis ofdata in a number of seasons. Identification of the varieties carrying asuperior combination of traits, which will give consistent yieldpotential, is a complex science. The desirable genotypic traits in thevariety can often be masked by other plant traits, unusual weatherpatterns, diseases, and insect damage. One widely employed method ofidentifying a superior plant with such genotypic traits is to observeits performance relative to commercial and experimental plants inreplicated studies. These types of studies give more certainty to thegenetic potential and usefulness of the plant across a number ofenvironments.

In summary, the goal of the soybean plant breeder is to produce new andunique soybeans and progeny of the soybeans for farmers' commercial cropproduction. To accomplish this, the plant breeder painstakingly crossestwo or more varieties or germplasm. Then the results of this cross arerepeatedly selfed or backcrossed to produce new genetic patterns. Neweravenues for producing new and unique genetic alleles in soybeans includeintroducing (or creating) mutations or transgenes into the geneticmaterial of the soybean are now in practice in the breeding industry.These genetic alleles can alter pest resistance such as diseaseresistance, insect resistance, nematode resistance, herbicideresistance, or they can alter the plant's environmental tolerances, orits seeds fatty acid compositions, the amount of oil produced, and/orthe amino acid/protein compositions of the soybean plant or its seed.

The traits a breeder selects for when developing new soybeans are drivenby the ultimate goal of the end user of the product. Thus if the goal ofthe end user is to resist a certain plant disease so overall more yieldis achieved, then the breeder drives the introduction of genetic allelesand their selection based on disease resistant levels shown by theplant. On the other hand, if the goal is to produce specific fatty acidcomposition, with for example a high level of oleic acid and/or a lowerlevel of linolenic acid, then the breeder may drive the selection ofgenetic alleles/genes based on inclusion of mutations or transgenes thatalter the levels of fatty acids in the seed. Reaching this goal mayallow for the acceptance of some lesser yield potential or other lessdesirable agronomic trait.

The new genetic alleles being introduced into soybeans are widening thepotential uses and markets for the various products and by-products ofthe oil from seed plants such as soybean. A major product extracted fromsoybeans is the oil in the seed. Soybean oil is employed in a number ofretail products such as cooking oil, baked goods, margarines and thelike. Another useful product is soybean meal, which is a component ofmany foods and animal feedstuffs.

SUMMARY OF THE INVENTION

One embodiment of the invention relates to seed of a soybean cultivardesignated AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104. The invention also relates to the plantfrom the seed designated AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104, the plant parts, or a plant cellof the soybean cultivar designated AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104. The invention alsoencompasses a tissue culture of regenerable cells, cells or protoplastsbeing from a tissue selected from the group consisting of: leaves,pollen, embryos, meristematic cells, roots, root tips, anthers, flowers,ovule, seeds, stems, pods, petals and the cells thereof.

The invention in one aspect covers a soybean plant, or parts thereof, ora cell of the soybean plant, having all of the physiological andmorphological characteristics of the soybean variety of the invention.

Another aspect of this invention is the soybean plant seed or derivedprogeny which contains a transgene which provides herbicide resistance,fungal resistance, insect resistance, resistance to disease, resistanceto nematodes, male sterility, or which alters the oil profiles, thefatty acid profiles, the amino acids profiles or other nutritionalqualities of the seed.

Another aspect of the current invention is a soybean plant furthercomprising a single locus conversion. In one embodiment, the soybeanplant is defined as comprising the single locus conversion and otherwisecapable of expressing all of the morphological and physiologicalcharacteristics of soybean variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104. In particularembodiments of the invention, the single locus conversion may comprise atransgenic gene which has been introduced by genetic transformation intothe soybean variety AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 or a progenitor thereof. In stillother embodiments of the invention, the single locus conversion maycomprise a dominant or recessive allele. The locus conversion maycomprise potentially any trait upon the single locus converted plant,including male sterility, herbicide resistance, disease resistance,insect resistance, modified fatty acid metabolism, modified carbohydratemetabolism, abiotic stress tolerance, drought tolerance, stresstolerance, modified nutrient deficiency tolerances, or resistance tobacterial disease, fungal disease, nematode disease, or viral disease.The single locus conversion may comprise phytase, fructosyltransferase,levansucrase, alpha-amylase, invertase, starch branching enzyme, or forexample, may encode an antisense of stearyl-ACP desaturase. The locusconversion may confer herbicide tolerance, where the tolerance isconferred to an herbicide selected from the group consisting ofglyphosate, glufosinate, acetolactate synthase (ALS) inhibitors,hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors, protoporphyrinogenoxidase (PPO) inhibitors, phytoene desaturase (PDS) inhibitors,photosystem II (PSII) inhibitors, dicamba and 2,4-D. The locusconversion may comprise QTLs which may affect a desired trait.

The locus conversion may also comprise a site-specific recombinationsite, such as an FRT site, Lox site, and/or other recombination sitesfor site-specific integration. This includes the introduction of atleast one FRT site that may be used in the FLP/FRT system and/or a Loxsite that may be used in the Cre/Lox system. For example, see Lyznik etal. (2003) Plant Cell Rep 21:925-932; and WO99/25821, which are herebyincorporated by reference. Other systems that may be used include theGin recombinase of phage Mu (Maeser et al. (1991) Mol Gen Genet230:170-176); the Pin recombinase of E. coli (Enomoto et al. (1983) JBacteriol 156:663-668); and the R/RS system of the pSRI plasmid (Arakiet al. (1992) J Mol Biol 182:191-203).

This invention embodies a method of introducing a desired trait, or ofsingle locus conversion, into soybean variety derived from AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104wherein the method comprises: (a) crossing a AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 plant witha plant of another soybean variety that comprises the locus or desiredtrait to produce F1 progeny plants; (b) selecting one or more F1 progenyplants from step (a) that have the desired trait or locus to produceselected progeny plants; (c) selfing the selected progeny plants of step(b) or crossing the selected progeny plants of step (b) with theAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 plants to produce late generation selected progeny plants; (d)crossing or further selecting for later generation selected progenyplants that have the desired trait or locus and physiological andmorphological characteristics of soybean variety AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 to produceselected next later generation progeny plants; and optionally (e)repeating crossing or selection of later generation progeny plants toproduce progeny plants that comprise the desired trait or locus and allof the physiological and morphological characteristics of said desiredtrait and of soybean variety AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 when grown in the same locationand in the same environment. The locus or desired trait may confer malesterility, herbicide resistance, disease resistance, insect resistance,modified fatty acid metabolism, modified carbohydrate metabolism, orresistance to bacterial disease, fungal disease or viral disease.

The present invention further provides a method for producing a soybeanseed with the steps of crossing at least two parent soybean plants andharvesting the hybrid soybean seed, wherein at least one parent soybeanplant is the present invention. Another aspect of the invention providesthe hybrid soybean seed and the progeny soybean plant and resultantseed, or parts thereof from the hybrid seed or plant or its progeny,including a plant cell from the hybrid plant or its progeny.

In an additional aspect, the invention covers a method for producing asoybean progeny from the invention by crossing soybean line AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104with a second soybean plant to yield progeny soybean seed and thengrowing progeny soybean seed to develop a derived soybean line.

Yet another aspect of the invention covers a method for a breedingprogram using plant breeding techniques which employ the soybean plantAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 as plant breeding material and performing breeding byselection techniques, backcrossing, pedigree breeding, marker enhancedselection, locus conversion, mutation and transformation. A single locusconversion of a site-specific recombination system allows for theintegration of multiple desired traits at a known recombination site inthe genome.

In an additional aspect, the invention covers a method for producing aninbred soybean plant derived from soybean variety AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 by crossingsoybean line AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 with a second soybean plant to yield progenysoybean seed, and then growing a progeny plant and crossing said plantwith itself or a second progeny plant to produce a progeny plant of asubsequent generation, and then repeating these steps for furthersubsequent generations to produce an inbred soybean plant derived fromsoybean variety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104.

In another aspect, the invention covers the plant produced by themethods described above, or a selfed progeny thereof, wherein the plantor selfed progeny comprises the desired trait, single locus, or loci andotherwise comprises essentially all of the physiological andmorphological characteristics of soybean variety AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 when grownin the same location and in the same environment.

DETAILED DESCRIPTION

The following data Is used to describe and enable the present soybeaninvention.

Common Name Code Name Description Cyst Nematode CN14R CN14R GreenhouseCyst Nematode Race 14 Race 14 1 = R, 3 = MR, CN14R 5 = seg, 9 = S CystNematode CN3_R CN3_R Greenhouse Cyst Nematode Race 3 CN3_R Race 3 1 = R,3 = MR, 5 = seg, 9 = S Dead Leaves DL__R DL__R Dead Leaves Rating (whennot sure what cause) Early Plot EPA_R Early Plot Appearance— Appearanceemergence, evenness of stand V2-V6 Emergence EMRGR Emerge Emergence 1 to9 (1 = best) EMRGR Flower Color FL_CR FL_CR Flower Color 1 = W = White;FL_CR 2 = P = Purple; 9 = Seg = Segregating (Mixture of Colors) FrogeyeLeaf FELSR FELS Frogeye Leaf Spot rating 1-9 Spot (1 = best) Grain YieldYGHMN YGHMN Grain Yield at Harvest at harvest Moisture moisture GrainYield at YGSMN Yield Grain Yield at Standard Std MST Moisture—(Qt/H)Green Lodging GLDGR GrLod Green Lodging Rating R5 to GLDGR R6 1 = Allerect; 5 = 45 degree; 9 = flat Green Stem GS__R GrnStem Green Stemrating 1-9 GS__R (1 = best) Harvest HVAPR HVAPR Overal HarvestAppearance Appearance 1 = best; 5 = average; 9 = Poor Harvest HLDGRHrvstLod Harvest Lodging 1 = All erect; Lodging 5 = 45 degree; 9 = flatHLDGR Hilum Color HILCT HILCT Hilum Color G = Grey; BR = Brown; BF =Buff; BL = Black; IB = Imperfect Black; Y = Yellow; IY = ImperfectYellow; S = Segregating (Mixture of Colors) Maturity Date MRTYD MRTYDMaturity Date (MMDD)— (MMDD) 95% of plants in row shed leaves & podsturned mature color Maturity Days MRTYN MatDays Maturity—Days from fromplanting planting date Moisture % GMSTP GMSTP Moisture % (Field) (Field)MST_P Phytophthora PRR_R PRR Phytophthora Root Rot Field Root RotTolerance. Rating (1 = best) Plant PLBRR Branch Plant Branching RatingBranching 1 = No branching; 5 = Average; 9 = Profuse Plant Canopy PLCNRCanopy Plant Canopy Rating PLCNR Rating 1 = no branching, 5 = average, 9= profuse Plant Height PLHTN Height Plant Height in centimeters (cm) PodColor PD_CR PD_CR Pod Color Rating 1 = T = Tawny; 2 = B = Brown; 9 = Seg= Segregating (Mixture of Colors) PRR GENE RPS_T RPS_T Phytophthora RootRot GENE, RPS_T 1C, 1K, No Gene, etc. Pubescence PB_CR PB_CR PubescenceColor Rating Color 1 = G = Gray; 2 = T = Tawny; 4 = Lt = Ligh Tawny; 9 =Seg = Segregating (Mixture of Colors) Root Knot MI_T MI_T Root KnotIncogita trait. R = Incogita resistance; MR = mixed resistance; S =susceptible Root Knot MI_R MI_R Root Knot Incognita rating Incognita (1= best) SCN Race CN14P CN14P Soybean Cyst Nematode Race 14 FI % 14Female Index % SCN Race CN3_P CN3_P Soybean Cyst Nematode Race 3 FI % 3FI % Shattering STR_R Shattering 1-9 (1 = best) Sulfonylurea STS_R STS_RSulfonylurea Tolerance Rating Tol. 1-9; 1 = Tolerant 9 = sensitive YieldTest TESTP ESTE The Mean Yield of the variety, Percentage expressed as apercentage of the Mean Yield of all varieties in the trialVariety/Hybrid VHNO VHNO A code designating a particular Number varietyIron Chlorosis IC_R Iron Chlorosis Rating or Calculated from Flash &Recovery Mean 1-9 (1 = best) Iron Chlorosis ICFLR Iron Chlorosis YellowYellow Flash Rating Flash Rate 1-9 (1 = best) Iron Chlorosis ICR_R IronChlorosis Recovery Rating Recovery 1-9 (1 = best) Radiometry IC_N IronDeficiency Chlorosis IDC Number Adjusted Radiometry Number Calculatedfrom Max Flast and Recovery Mean Brown Stem BSR_R BSR Brown Stem RotRating 1-9 Rot (1 = best) Charcoal Rot CR_R Charcoal Rot Rating 1-9 (1 =best) Powdery PM_R Powdery Mildew Rating 1-9 Mildew (1 = best) BacterialBP_R Bacterial Pustule Rating 1-9 Pustule (1 = best) Rust RUSTR Rustseverity overall rating 1-9, 9 being higher severity Sudden Death SDS_RSudden Death Syndrome Rating Syndrome 1-9 (1 = best) Sclerotinia SCL_RSWM Sclerotinia White Mold Severity White Mold Rating 1-9 (1 = best)Target Spot TSP_R Target Spot (Corynespora cassiicola) Rating 1-9 (1 =best) Stem Canker DPM_R Stem Canker (Southern) Rating (Southern) 1-9 (1= best) Stem Canker DPMTR Stem Canker (Southern) (South) ToleranceRating 1-9 (1 = best) Tolerance

Trait Definitions

Hypocotyl Length (Hyp_R) A rating of a variety's hypocotyl extensionafter germination when planted at a 5″ depth in sand and maintained in awarm germination environment for 10 days.

Leaf Shape Calculated A calculated trait that divides length by widthamongst 5 different leaf samples per replicate, measured in cm.1=lanceolate; 2=oval; 3=ovate.

Seedling Establishment (EMRGR) A rating of uniform establishment andgrowth of seedlings. Rating is taken between the V1 and V3 growth stagesand is a 1 to 9 rating with 1 being the best stand establishment.

Seed Coat Peroxidase (Perox)—seed protein peroxidase activity is achemical taxonomic technique to separate cultivars based on the presenceor absence of the peroxidase enzyme in the seed coat. Ratings arePOS=positive for peroxidase enzyme or NEG=negative for peroxidaseenzyme. Ratings may also refer to the activity level of the seed proteinperoxidase. 1=low activity; 2=high activity.

Chloride Sensitivity (CLS_T) An “Excluder” accumulates chloride andrestricts the chloride in the roots. An “Includer” accumulates chloridethroughout the plant. Based on molecular markers for analyzing chloridesensitivity, a chloride excluder carries a susceptible marker allele,and a chloride includer has a resistant allele.

Plant Height (PLHTN) The average measured plant height, in centimeters,of 5 uniform plants per plot, taken just prior to harvest.

Plant Branching (PLBRR) Rating of the number of branches and theirrelative importance to yield. This rating is taken at growth expressivelocations. 1=no branching, 5=average and 9=profuse. Ratings taken justprior to harvest. Green Lodging (GLDGR) Rating based on the average ofplants leaning from vertical at the R5 to R6 growth stage. 1=all areerect, 5=average erectness. 9=all are flat. Rating of one is the bestrating.

Harvest Lodging (HLDGR) Rating based on the average of plants leaningfrom vertical at harvest. Lodging score (1=completely upright, 5=45degree angle from upright; 9=completely prostrate). Rating one is thebest rating and ratings are taken just prior to harvest.

MON89788 The transgenic soybean event MON89788 carries a glyphosatetolerance transgene (U.S. Pat. No. 7,632,985 herein incorporated byreference). This transgene may be introgressed into a soybean variety,such that said variety now carries a glyphosate tolerance transgene.

MON87708 The transgenic soybean event MON87708 carries a transgene whichexpresses a dicamba mono-oxygenase, which confers tolerance todicamba-based herbicides. This transgene may be introgressed into asoybean variety, such that said variety now carries a dicamba tolerancetransgene.

Phytophthora Root Rot (PRR_R) means a Phytophthora Root Rot fieldtolerance rating. Rating is 1-9 with one being the best. The informationcan also include the listing of the actual resistance gene (RPS_T), forexample, Rps gene 1C.

Root Knot Nematode (RKN) Greenhouse screen—45 day screen of rootsinoculated with eggs and juveniles. Rating Scale based upon femalereproduction index on a susceptible check set determined by number ofgalls present on the root mass. Rating scale is 1-9 with 1 being best.Species specific ratings: Arenaria (MA_R), Incognita (MI_R), Javanica(MJ_R).

Stem Canker (Southern) (DPM_R) Greenhouse screen to identify vertical(gene) type of resistance. One week old soybean seedlings are inoculatedwith the stem canker pathogen by opening up a small slit into thehypocotyl and depositing a small drop of the fungal suspension. Theinoculated seedlings are then placed into a moisture chamber. When theseedlings of the known checks have collapsed, disease severity ratingare given on a 1-9 score. One being the best.

Stem canker (Southern) tolerance (DPMTR) Field nursery. The objective ofthis test is to evaluate the Field Resistance/Tolerance of soybean linesunder field conditions. This is necessary due to the fact that of thefour known genes that convey vertical type of resistance to stem canker,one gene (Rdc4 from the variety Dowling), exhibits a 40-50% plant kill(false positive) when screened in the greenhouse using the hypocotylinoculation technique. Lines that scored a rating of 4-9 in thegreenhouse are planted in the field. They are sprayed at least 5 timesduring their first month of development with a spore suspensioncontaining the stem canker fungus. With the inclusion of verysusceptible stem canker checks, we are able to identify horizontal(field resistance/tolerance) resistance in certain lines. Quite often,lines scoring a 9 in the greenhouse, rate a score of 1 in the field dueto either having the Rdc4 gene or having good fieldresistance/tolerance. Disease severity scores are once again given on a1-9 scale when the plants have reached the R6 growth stage of plantdevelopment. One being the best.

Brown Stem Rot (BSR_R) This disease is caused by the fungus Phialophoragregata. The disease is a late-season, cool-temperature, soil bornefungus which in appropriate favorable weather can cause up to 30 percentyield losses in soybean fields. BSR_R is an opportunistic field rating.The scale is 1-9. One rating is best.

Sudden Death Syndrome (SDS_R) This disease is caused by slow-growingstrains of Fursarium solani that produce bluish pigments in the centralpart of the culture when produced on a PDA culture. The disease appearsmainly in the reproductive growth stages (R2-R6) of soybeans. Normaldiagnostics are distinctive scattered, interveinal chlorotic spots onthe leaves. Yield losses may be total or severe in infected fields. TheSudden Death Syndrome Rating is both a field nursery and anopportunistic field rating. It is based on leaf area affected as definedby the Southern Illinois University method of SDS scoring. The scaleused for these tests is 1-9. A one rating is best.

Sclerotinia White Mold (SCL_R) This disease is caused by the fungalpathogen Sclerotinia sclerotium. The fungus can overwinter in the soilfor many years as sclerotia and infect plants in prolonged periods ofhigh humidity or rainfall. Yield losses may be total or severe ininfected fields. Sclerotinia White Mold (SCL_R) rating is a field rating(1-9 scale) based on the percentage of wilting or dead plants in a plot.A one rating is the best.

Frog Eye Leaf Spot (FELSR) This is caused by the fungal pathogenCercospora sojina. The fungus survives as mycelium in infected seeds andin infested debris. With adequate moisture new leaves become infected asthey develop until all the leaves are infected. Yield losses may be upto 15% in severe infected fields. Frog Eye Leaf Spot (FELSR) rating is afield rating (1-9 scale) based on the percentage of leaf area affected.The scale is 1-9 where 1=no leaf symptoms and 9=severe leaf symptoms.One is the best rating. To test varieties for Frog Eye Leaf Spot adisease nursery is artificially inoculated with spores. The ratings aredone when the plants have reached the R5-R6 growth stage. Visualcalibration is done with leaf photos of different frogeye severityratings as used by the University of Tennessee and Dr. Melvin Newman,State Plant Pathologist for TN.

Soybean Cyst Nematode (SCN) The Soybean Cyst Nematode Heteroderaglycines, is a small plant-parasitic roundworm that attacks the roots ofsoybeans. Soybean Cyst Nematode Ratings are taken from a 30 daygreenhouse screen using cyst infested soil. The rating scale is basedupon female reproduction index (FI %) on a susceptible check set((female reproduction on a specific line/female reproduction onSusceptible check)*100) where <10%=R (RESISTANT); >10%-<30%=MR(MODERATELY RESISTANT); >30%-<60%=MS (MODERATELY SUSPECTIBLE); >60%=S(SUSPECTIBLE). The screening races include: 1, 3, 5, 14. Individualratings CN1_P, CN3_P, CN5_P, and CN14_P refer to the resistance to SCNraces 1, 3, 5 and 14 FI % respectively.

Powdery Mildew The name given to a group of diseases caused by severalclosely related fungi. Their common symptom is a grayish-white, powderymat visible on the surface of leaves, stems, and flower petals. Thereare many hosts; and although this disease is not considered fatal, plantdamage can occur when the infestation is severe.

Soybean Rust (Rust) Previously known as Asian soybean rust. This diseaseis caused by the fungus Phakopsora pachyrhiz.

Maturity Days from Planting (MRTYN) Plants are considered mature when95% of the pods have reached their mature color. MRTYN is the number ofdays calculated from planting date to 95% mature pod color.

Relative Maturity Group (RM) Industry Standard for varieties groups,based on day length or latitude. Long day length (northern areas in theNorthern Hemisphere) are classified as (Groups 000,00,0). Mid daylengths variety groups lie in the middle group (Groups I-VI). Very shortday lengths variety groups (southern areas in Northern Hemisphere) areclassified as (Groups VII, VIII, IX). Within a maturity group aresub-groups. A sub-group is a tenth of a relative maturity group (forexample, 1.3 would indicate a group 1 and a subgroup 3). Within narrowcomparisons, the difference of a tenth of a relative maturity groupequates very roughly to a day difference in maturity at harvest.

Grain Yield at Standard Moisture (YGSMN) The actual grain yield atstandard moisture (13%) reported in the unit's bushels/acre.

Shattering (STR_R) The rate of pod dehiscence prior to harvest. Poddehiscence is the process of beans dropping out of the pods. Advancedvarieties are planted in a replicated nursery south of their adaptedzone to promote early senescence. Mature plots are allowed to stand inthe field to endure heat/cool and especially wet/dry cycles. Rating isbased on the differences between varieties of the amount of open podsand soybeans that have fallen on the ground. The rating scale is 1-9with 1=no shattering and 9=severe shattering. One rating is best.

Yield Test Percentage (TESTP) The mean yield of the subject varietyexpressed as a percentage of the mean yield of all varieties in thetrial.

Plant Parts Means the embryos, anthers, pollen, nodes, roots, root tips,flowers, petals, pistols, seeds, pods, leaves, stems, tissue, tissuecultures, meristematic cells and other cells (but only to the extent thegenetic makeup of the cell has both paternal and maternal material) andthe like.

Palmitic Acid Means a fatty acid, C₁₅H₃₁COOH, occurring in soybean. Thisis one of the five principal fatty acids of soybean oil.

Linolenic Acid Means an unsaturated fatty acid, C₁₇H₂₉COOH, occurring insoybean. This is one of the five principal fatty acids of soybean oil.

Stearic Acid Means a colorless, odorless, waxlike fatty acid,CH₃(CH₂)₁₆COOH, occurring in soybean. This is one of the five principalfatty acids of soybean oil.

Oleic Acid Means an oily liquid fatty acid, C₁₇H₃₃COOH, occurring insoybean. This is one of the five principal fatty acids of soybean oil.

Linoleic Acid Means an unsaturated fatty acid, C₁₇H₃₁COOH, occurring insoybean. This is one of the five principal fatty acids of soybean oil.

Plant Means the plant, in any of its stages of life including the seedor the embryo, the cotyledon, the plantlet, the immature or the matureplant, the plant parts, plant protoplasts, plant cells of tissue culturefrom which soybean plants can be regenerated, plant calli, plant clumps,and plant cells (but only to the extent the genetic makeup of the cellhas both paternal and maternal material) that are intact in plants orparts of the plants, such as pollen, anther, nodes, roots, flowers,seeds, pods, leaves, stems, petals and the like.

Bud Blight (virus—tobacco ringspot virus): A virus disease of soybeans,symptoms form a curled brown crook out of the terminal bud of plants.

Soybean Mosaic (virus): This soybean virus appears as a yellow vein oninfected plants. This virus will show in the veins of developing leaves.Leaves look narrow and have puckered margins. Infection results in lessseed formed in odd shaped pods. The virus is vectored by aphids.

Bean Pod Mottle Virus (virus): The bean leaf beetle vectored virus. Thisvirus causes a yellow-green mottling of the leaf particularly in coolweather.

Target Spot (fungus—Alternaria sp.): This fungus infects leaves, alsoshows spots on pods and stems.

Anthracnose (fungus—Colletotrichum dematium var. truncatum): This fungusinfects stems, petioles and pods of almost mature plants.

Brown Leaf Spot (fungus—Septoria glycines): Early foliar disease onsoybeans in springtime.

Downy Mildew (fungus—Peronospora manshurica): Fungus appears on thetopside of the leaf. The fungus appears as indefinite yellowish-greenareas on the leaf.

Purple Seed Stain (fungus—Cercospora kikuchii): This fungus is on themature soybean seed coat and appears as a pink or light to dark purplediscoloration.

Seed Decay and Seedling Diseases (fungi—Pythium sp., Phytophthora sp.,Rhizoctonia sp., Diaporthe sp.): When damage or pathology causes reducedseed quality, then the soybean seedlings are often predisposed to thesedisease organisms.

Bacterial Blight (bacterium—Pseudomonas syringae pv. glycinea): Asoybean disease that appears on young soybean plants.

Charcoal Rot (fungus—Macrophomina phaseolina): Charcoal rot is a sandysoil, mid-summer soybean disease.

Rhizoblum—Induced Chlorosis: A chlorosis appearing as light green towhite which appears 6-8 weeks during rapid plant growth.

Bacterial Pustule (bacterium—Xanthomonas campestris pv. phaseoli): Thisis usually a soybean leaf disease; however, the disease from the leavesmay infect pods.

Cotton Root Rot (fungus—Phymatotrichum omnivorum): This summertimefungus causes plants to die suddenly.

Pod and Stem Blight (fungus—Diaporthe phaseolorum var. sojae): Thefungus attacks the maturing pod and stem and kills the plant.

Treated Seed means the seed of the present invention with a pesticidalcomposition. Pesticidal compositions include but are not limited tomaterial that are insecticidal, fungicidal, detrimental to pathogens, orsometimes herbicidal.

Locus converted (conversion), also single locus converted (conversion),refers to seeds, plants, and/or parts thereof developed by backcrossingand/or genetic transformation to introduce a given locus that istransgenic in origin, wherein essentially all of the morphological andphysiological characteristics of a variety are recovered in addition tothe characteristics of the locus or possibly loci which has beentransferred into the variety. The locus can be a native locus, atransgenic locus, or a combination thereof. Plants may also be referredto as coisogenic plants.

Variety or Cultivar refer to a substantially homozygous soybean line andminor modifications thereof that retains the overall genetics of thesoybean line including but not limited to a subline, a locus conversion,a mutation, a transgenic, or a somaclonal variant. Variety or cultivarinclude seeds, plants, plant parts, and/or seed parts of the instantsoybean line.

Definitions of Staging of Development

The plant development staging system employed in the testing of thisinvention divides stages as vegetative (V) and reproductive (R). Thissystem accurately identifies the stages of any soybean plant. However,all plants in a given field will not be in the stage at the same time.Therefore, each specific V or R stage is defined as existing when 50% ormore of the plants in the field are in or beyond that stage.

The first two stages of V are designated a VE (emergence) and VC(cotyledon stage). Subdivisions of the V stages are then designatednumerically as V1, V2, V3 through V (n). The last V stage is designatedas V (n), where (n) represents the number for the last node stage of thespecific variety. The (n) will vary with variety and environment. Theeight subdivisions of the reproductive stages (R) states are alsodesignated numerically. R1=beginning bloom; R2=full bloom; R3=beginningpod; R4=full pod; R5=beginning seed; R6=full seed; R7=beginningmaturity; R8-full maturity.

Soybean Cultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104

The present invention comprises a soybean plant, plant part, plant cell,and seed, characterized by molecular and physiological data obtainedfrom the representative sample of said variety deposited with theAmerican Type Culture Collection. Additionally, the present inventioncomprises a soybean plant comprising the homozygous alleles of thevariety, formed by the combination of the disclosed soybean plant orplant cell with another soybean plant or cell.

This soybean variety in one embodiment carries one or more transgenes,for example, the glyphosate tolerance transgene, a dicambamono-oxygenase gene, a desaturase gene or other transgenes. In anotherembodiment of the invention, the soybean does not carry any herbicideresistance traits. In yet another embodiment of the invention, thesoybean does not carry any transgenes but may carry alleles for aphidresistance, cyst nematode resistance and/or brown stem rot or the like.

The present invention provides methods and composition relating toplants, seeds and derivatives of the soybean cultivar AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104.Soybean cultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 has superior characteristics. The AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104line has been selfed sufficient number of generations to provide astable and uniform plant variety.

Cultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 shows no variants other than expected due toenvironment or that normally would occur for almost any characteristicduring the course of repeated sexual reproduction. Some of the criteriaused to select in various generations include: seed yield, emergence,appearance, disease tolerance, maturity, plant height, and shatteringdata.

The inventor(s) believe that AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 are similar in relative maturityto the comparison varieties. However, as shown in the tables and asdescribed, AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 differs from these cultivars.

Direct comparisons were made between AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104 and the listednon-commercial or commercial varieties. Traits measured may includeyield, maturity, lodging, plant height, branching, field emergence, andshatter. The results of the comparison are presented in the followingtables. The number of tests in which the varieties were compared isshown with the environments, mean and standard deviation for sometraits.

It is well known in the art that, by way of backcrossing, one or moretraits or loci may be introduced into a given variety while otherwiseretaining essentially all of the traits of that variety. An example ofsuch backcrossing to introduce a trait into a starting variety isdescribed in U.S. Pat. No. 6,140,556, where soybean variety Williams '82was developed using backcrossing techniques to transfer a locuscomprising the Rps1 gene to the variety Williams. Williams '82 iscomparable to the recurrent parent variety Williams except forresistance to phytopthora rot. Both Williams '82 and Williams have thesame relative maturity, indeterminate stems, and flower, pod,pubescence, and hilum color.

AR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 can carry genetic engineered recombinant genetic material togive improved traits or qualities to the soybean. For example, but notlimited to, AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 can carry the glyphosate resistance gene forherbicide resistance as taught in the Monsanto patents (WO92/00377,WO92/04449, U.S. Pat. Nos. 5,188,642 and 5,312,910), or a gene whichconfers tolerance to dicamba-based herbicides, or the STS mutation forherbicide resistance. Additional traits carried in transgenes ormutation can be transferred into AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104. Some of these genesinclude genes that give disease resistance to sclerotinia such as theoxalate oxidase (Ox Ox) gene as taught in PCT/FR92/00195 Rhone Poluncand/or an oxalate decarboxylase gene for disease resistance or genesdesigned to alter the soybean oil within the seed such as desaturase,thioesterase genes (shown in EP0472722, U.S. Pat. No. 5,344,771) orgenes designed to alter the soybean's amino acid characteristics. Thisline can be crossed with another soybean line which carries a gene thatacts to provide herbicide resistance or alter the saturated and/orunsaturated fatty acid content of the oil within the seed, or the aminoacid profile of the seed. Thus through transformation or backcrossing ofthe present varieties with a transgenic line carrying the desired event,the present invention further comprise a new transgenic event that isheritable. Some of the available soybean transgenic events include11-234-01p Dow Soybean 2, 4-D, Glyphosate and GlufosinateTolerant/DAS-444Ø6-6; 11-202-01p Monsanto Soybean Increased Yield/MON87712; 10-188-01p Monsanto Soybean Dicamba Tolerant/MON 87708;09-015-01p BASF Soybean Imadazolinone Tolerant/BPS-CV127-9; 09-328-01pBayer Soybean Glyphosate and Isoxaflutole Tolerant/FG72; 09-201-01pMonsanto Soybean Improved Fatty Acid Profile/MON 87705; 09-183-01pMonsanto Soybean Stearidonic Acid Produced/MON 87769; 09-082-01pMonsanto Soybean Insect Resistant/MON 87701; 06-354-01p Pioneer SoybeanHigh Oleic Acid/Event 305423; 06-271-01p Pioneer Soybean Glyphosate &Acetolactate Synthase Tolerant/DP-356043-5; 06-178-01p Monsanto SoybeanGlyphosate Tolerant/MON 89788; 98-238-01p AgrEvo SoybeanPhosphinothricin Tolerant/GU262; 97-008-01p Du Pont Soybean High OleicAcid Oil/G94-1, G94-19, G-168; 96-068-01p AgrEvo Soybean GlufosinateTolerant/W62, W98, A2704-12, A2704-21, A5547-35; 96-068-01p AgrEvoSoybean Glufosinate Tolerant/W62, W98, A2704-12, A2704-21, A5547-35;93-258-01p Monsanto Soybean Glyphosate Tolerant/4-30-2.

The present varieties and/or their progeny can also carry herbicidetolerance where the tolerance is conferred to an herbicide selected fromthe group consisting of glyphosate, glufosinate, acetolactate synthase(ALS) inhibitors, hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors,protoporphyrinogen oxidase (PPO) inhibitors, phytoene desaturase (PDS)inhibitors, photosystem II (PSII) inhibitors, dicamba and 2,4-D.

This invention also is directed to methods for producing a new soybeanplant by crossing a first parent plant with a second parent plantwherein the first or second parent plant is AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 or progenythereof. Additionally, the present varieties and/or their progeny may beused in the variety development process to derive progeny in a breedingpopulation or crossing. Further, both first and second parent plants canbe or be derived from the soybean line AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104. A variety of breedingmethods can be selected depending on the mode of reproduction, thetrait, the condition of the germplasm. Thus, any such methods using theAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 are part of this invention: selfing, backcrosses, locusconversion, recurrent selection, mass selection and the like.

The scope of the present invention includes use of marker methods. Inaddition to phenotypic observations, the genotype of a plant can also beexamined. There are many techniques or methods known which are availablefor the analysis, comparison and characterization of plant's genotypeand for understanding the pedigree of the present invention andidentifying plants that have the present invention as an ancestor; amongthese are Isozyme Electrophoresis, Restriction Fragment LengthPolymorphisms (RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs),Arbitrarily Primed Polymerase Chain Reaction (AP-PCR), DNA AmplificationFingerprinting (DAF), Sequence Characterized Amplified Regions (SCARs),Amplified Fragment Length Polymorphisms (AFLPs), and Simple SequenceRepeats (SSRs) which are also referred to as Microsatellites.

A genotypic profile of soybean variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104 can be used toidentify a plant comprising variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104 as a parent, sincesuch plants will comprise the same homozygous alleles as varietyAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104. Because the soybean variety is essentially homozygous at allrelevant loci, most loci should have only one type of allele present. Incontrast, a genetic marker profile of an F1 progeny should be the sum ofthose parents, e.g., if one parent was homozygous for allele X at aparticular locus, and the other parent homozygous for allele Y at thatlocus, then the F1 progeny will be XY (heterozygous) at that locus.Subsequent generations of progeny produced by selection and breeding areexpected to be of genotype XX (homozygous), YY (homozygous), or XY(heterozygous) for that locus position. When the F1 plant is selfed orsibbed for successive filial generations, the locus should be either Xor Y for that position.

In addition, plants and plant parts substantially benefiting from theuse of variety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 in their development, such as varietyAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104 comprising a backcross conversion, locus conversion,transgene, or genetic sterility factor, may be identified by having amolecular marker profile with a high percent identity to soybean varietyAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104. Such a percent identity might be 90%, 91%, 92%, 93%, 94%,95%, 96%, 97%, 98%, 99%, 99.5% or 99.9% identical to soybean varietyAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104.

A genotypic profile of variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104 also can be used toidentify essentially derived varieties and other progeny varietiesdeveloped from the use of variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104, as well as cells andother plant parts thereof. Plants of the invention include any planthaving at least 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%,or 99.9% of the markers in the genotypic profile, and that retain 90%,91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, 99.5%, or 99.9/a of themorphological and physiological characteristics of variety AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104when grown under the same conditions. Such plants may be developed usingmarkers well known in the art. Progeny plants and plant parts producedusing variety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 may be identified, for example, by having amolecular marker profile of at least 25%, 30%, 35%, 40%, 45%, 50%, 55%,60%, 65%, 70%, 75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%,86%, 87%, 88%, 89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99%, or99.5% genetic contribution from soybean variety AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104, asmeasured by either percent identity or percent similarity. Such progenymay be further characterized as being within a pedigree distance ofvariety AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104, such as within 1, 2, 3, 4, or 5 or lesscross pollinations to a soybean plant other than variety AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104,or a plant that has variety AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 as a progenitor. Unique molecularprofiles may be identified with other molecular tools, such as SNPs andRFLPs.

The present invention also includes methods of isolating nucleic acidsfrom a plant, a plant part, or a seed of the soybean variety of theinvention, analyzing said nucleic acids to produce data, and recordingsaid data. In some embodiments, the data may be recorded on a computerreadable medium. The data may comprise a nucleic acid sequence, a markerprofile, a haplotype, or any combination thereof. In some embodiments,the data may be used for crossing, selection, or advancement decisionsin a breeding program.

A backcross conversion, locus conversion, transgene, or geneticsterility factor, may be in an embodiment of the present invention.Markers can be useful in their development, such that the presentinvention comprising backcross conversion(s), transgene(s), or geneticsterility factor(s), and are identified by having a molecular markerprofile with a high percent identity such as 95%, 96%, 97%, 98%, 99%,99.5% or 99.9% identical to AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104

These embodiments may be detected using measurements by either percentidentity or percent similarity to the deposited material. These markersmay detect progeny plants identifiable by having a molecular markerprofile of at least 25%, 30%, 35%, 40%, 45%, 50%, 55%, 60%, 65%, 70%,75%, 76%, 77%, 78%, 79%, 80%, 81%, 82%, 83%, 84%, 85%, 86%, 87%, 88%,89%, 90%, 91%, 92%, 93%, 94%, 95%, 96%, 97%, 98%, 99% or 99.5% geneticcontribution from an embodiment of the present soybean varietiesAR1403091, EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/orEE1761104. Such progeny may be further characterized as being within apedigree distance of 1, 2, 3, 4 or 5 or more cross-pollinations to asoybean plant other than the present varieties or a plant that has oneof the present varieties as a progenitor. Molecular profiles may beidentified with SNP, Single Nucleotide Polymorphism, or other toolsalso.

Traits are average values for all trial locations, across all years inwhich the data was taken. In addition to the visual traits that aretaken, the genetic characteristic of the plant can also be characterisedby its genetic marker profile. The profile can interpret or predict thepedigree of the line, the relation to another variety, determine theaccuracy of a listed breeding strategy, or invalidate a suggestedpedigree. Soybean linkage maps were known by 1999 as evidenced in Creganet. al, “An Integrated Genetic Linkage Map of the Soybean Genome” CropScience 39:1464 1490 (1999); and using markers to determine pedigreeclaims was discussed by Berry et al., in “Assessing Probability ofAncestry Using Simple Sequence Repeat Profiles: Applications to MaizeInbred Lines and Soybean Varieties” Genetics 165:331 342 (2003), each ofwhich are incorporated by reference herein in their entirety. Markersinclude but are not limited to Restriction Fragment Length Polymorphisms(RFLPs), Randomly Amplified Polymorphic DNAs (RAPDs), Arbitrarily PrimedPolymerase Chain Reaction (AP-PCR), DNA Amplification Fingerprinting(DAF), Sequence Characterized Amplified Regions (SCARs), AmplifiedFragment Length Polymorphisms (AFLPs), Simple Sequence Repeats (SSRs)which are also referred to as Microsatellites, and Single NucleotidePolymorphisms (SNPs). There are known sets of public markers that arebeing examined by ASTA and other industry groups for their applicabilityin standardizing determinations of what constitutes an essentiallyderived variety under the US Plant Variety Protection Act. However,these standard markers do not limit the type of marker and markerprofile which can be employed in breeding or developing backcrossconversions, or in distinguishing varieties or plant parts or plantcells, or verify a progeny pedigree. Primers and PCR protocols forassaying these and other markers are disclosed in the Soybase (sponsoredby the USDA Agricultural Research Service and Iowa State University)located at the world wide web at 129.186.26.94/SSR.html.

Additionally, these markers such as SSRs, RFLP's, SNPs, Ests, AFLPs,gene primers, and the like can be developed and employed to identifygenetic alleles which have an association with a desired trait, loci orlocus. The allele can be used in a marker assisted breeding program tomove traits (native, nonnative (from a different species), ortransgenes) into AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104, or progeny thereof. The value of markersincludes allowing the introgression and/or locus conversion of theallele(s)/trait(s) into the desired germplasm with little to nosuperfluous germplasm being dragged from the allele/trait donor plantinto the present varieties or progeny thereof. This results in formationof, for example, cyst nematode resistance, brown stem rot resistance,aphid resistance, Phytophthora resistance, IDC resistance, BT genes,male sterility genes, glyphosate tolerance genes, Dicamba tolerance,HPPD tolerance, rust tolerance, Asian Rust tolerance, fungal tolerance,or drought tolerance genes. Additionally, the present varieties orprogeny thereof through transgenes, or if a native trait through markersor backcross breeding, can include a polynucleotide encoding phytase,FAD-2, FAD-3, galactinol synthase or a raffinose synthetic enzyme; or apolynucleotide conferring resistance to soybean cyst nematode, brownstem rot, phytophthora root rot, or sudden death syndrome or resistance,tolerance to FUNGAL DISEASES such as: Alternaria spp., Agrobacteriumrhizogenes, Calonectria crotalariae, Cercospora kikuchii, Cercosporasojina, Choanephora infundibulifera, Colletotrichum spp., Corynesporacassiicola, Curtobacterium flaccumfaciens, Dactuliochaeta glycines,Diaporthe phaseolorum, Fusarium oxysporum, Macrophomina phaseolina,Microsphaera difusa, Peronospora manshurica, Phakopsora pachyrhizi,Phialophora gregata, Phomopsis phaseolorum, Phyllosticta sojicola,Phytophthora sojae, Pseudomonas syringae, Pythium spp., Rhizoctoniasolana, Sclerotinia sclerotiorum, Sclerotium rolfsii, Septoria glycines,Sphaceloma glycines, Thielaviopsis basicota; or tolerance to BACTERIALand VIRAL DISEASES such as: Xanthomonas campestres, Cowpea ChloroticMottle Virus (CCMV), Peanut Mottle Virus (PMV), Tobacco Streak Virus(TSV), Bean Yellow Mosaic Virus (BYMV), Black Gram Mottle Virus (BGMV),Cowpea Mild Mottle Virus (CMMV), Cowpea Severe Mosaic Virus (CSMV),Indonesian Soybean Dwarf Virus (ISDV), Mung Bean Yellow Mosaic Virus(MYMV), Peanut Stripe Virus (VPMM), Soybean Chlorotic Mottle Virus,Soybean Crinkle Leaf Virus, Soybean Yellow Vein Virus (SYVV), TobaccoMosaic Virus (TMV); NEMATODES such as: Belonolaimus gracilis,Meloidogyne spp, Rotylenchulus reniformis, Pratylenchus spp.,Hoplolaimus sulumbus, Heterodera schachtii.

Many traits have been identified that are not regularly selected for inthe development of a new cultivar. Using materials and methods wellknown to those persons skilled in the art, traits that are capable ofbeing transferred, to a cultivar of the present invention include, butare not limited to, herbicide tolerance, resistance for bacterial,fungal, or viral disease, nematode resistance, insect resistance,enhanced nutritional quality, such as oil, starch and protein content orquality, improved performance in an industrial process, alteredreproductive capability, such as male sterility or male/femalefertility, yield stability and yield enhancement. Other traits includethe production of commercially valuable enzymes or metabolites withinthe present invention.

A transgene typically comprises a nucleotide sequence whose expressionis responsible or contributes to the trait, under the control of apromoter capable of directing the expression of the nucleotide sequenceat the desired time in the desired tissue or part of the plant.Constitutive, tissue-specific or inducible promoters are well known inthe art and have different purposes and each could be employed. Thetransgene(s) may also comprise other regulatory elements such as forexample translation enhancers or termination signals. The transgene maybe adapted to be transcribed and translated into a protein, or to encodeRNA in a sense or antisense orientation such that it is not translatedor only partially translated.

Transgenes may be directly introduced into the cultivar using geneticengineering, site specific insertion techniques, and transformationtechniques well known in the art or introduced into the cultivar througha process which uses a donor parent which has the transgene(s) alreadyintrogressed. This process of introduction of a transgene(s) ornative/non-native traits into the cultivar may use the donor parent in amarker assisted trait conversion process, where the trait may be movedfor example by backcrossing using the markers for selection ofsubsequent generations.

The laboratory-based techniques described above, in particular RFLP andSSR, can be used in such backcrosses to identify the progenies havingthe highest degree of genetic identity with the recurrent parent. Thispermits one to accelerate the production of soybean cultivars having atleast 90%, 95%, 99% genetic, or genetically identical to the recurrentparent, and further comprising the trait(s) introgressed from the donorparent. Such determination of genetic identity can be based on markersused in the laboratory-based techniques described above.

The last backcross generation is then selfed to give pure breedingprogeny for the gene(s) being transferred. The resulting plants haveessentially all of the morphological and physiological characteristicsof a cultivar of the present invention, in addition to the gene trait(s)transferred to the inbred. The exact backcrossing protocol will dependon the trait being altered to determine an appropriate testing protocol.Although backcrossing methods are simplified when the trait beingtransferred is a dominant allele, a recessive allele may also betransferred. In this instance it may be necessary to introduce a test ofthe progeny to determine if the desired trait has been successfullytransferred.

In general, methods to transform, modify, edit or alter plant endogenousgenomic DNA include altering the plant native DNA sequence or apre-existing transgenic sequence including regulatory elements, codingand non-coding sequences. These methods can be used, for example, totarget nucleic acids to pre-engineered target recognition sequences inthe genome. Such pre-engineered target sequences may be introduced bygenome editing or modification. As an example, a genetically modifiedplant variety is generated using “custom” or engineered endonucleasessuch as meganucleases produced to modify plant genomes (see e.g., WO2009/114321; Gao et al. (2010) Plant Journal 1:176-187). Anothersite-directed engineering method is through the use of zinc fingerdomain recognition coupled with the restriction properties ofrestriction enzyme. See e.g., Umov, et al., (2010) Nat Rev Genet.11(9):636-46; Shukla, et al., (2009) Nature 459 (7245):437-41. Atranscription activator-like (TAL) elfector-DNA modifying enzyme (TALEor TALEN) is also used to engineer changes in plant genome. See e.g.,US20110145940, Cermak et al. (2011), Nucleic Acids Res. 39(12) and Bochet al., (2009), Science 326(5959): 1509-12. Site-specific modificationof plant genomes can also be performed using the bacterial type IICRISPR (clustered regularly interspaced short palindromic repeats)/Cas(CRISPR-associated) system. See e.g., Belhaj et al., (2013), PlantMethods 9: 39; The Cas9/guide RNA-based system and Cas12a/guideRNA-based system, for example, allow targeted cleavage of genomic DNAguided by a customizable small noncoding RNA in plants (see e.g., WO2015026883A1 and WO2016205711A1, each incorporated herein by reference).

The cultivars of the invention can also be used for transformation whereexogenous genes are introduced and expressed by the cultivars of theinvention. Genetic variants created either through traditional breedingmethods using a cultivar of the present invention or throughtransformation of such cultivar by any of a number of protocols known tothose of skill in the art are intended to be within the scope of thisinvention (see e.g. Trick et al. (1997) Recent Advances in SoybeanTransformation, Plant Tissue Culture and Biotechnology, 3:9-26).

Transformation methods are means for integrating new genetic codingsequences (transgenes) into the plant's genome by the incorporation ofthese sequences into a plant through man's assistance. Many dicotsincluding soybeans can easily be transformed with Agrobacterium. Methodsof introducing desired recombinant DNA molecule into plant tissueinclude the direct infection or co-cultivation of plant cells withAgrobacterium tumefaciens, Horsch et al., Science, 227:1229 (1985).Descriptions of Agrobacterium vector systems and methods are shown inGruber, et al., “Vectors for Plant Transformation, in Methods in PlantMolecular Biology & Biotechnology” in Glich et al., (Eds. pp. 89-119,CRC Press, 1993). Transformed plants obtained via protoplasttransformation are also intended to be within the scope of thisinvention. Other transformation methods such as whiskers, aerosol beam,etc. are well known in the art and are within the scope of thisinvention. The most common method of transformation after the use ofagrobacterium is referred to as gunning or microprojectile bombardment.This process has small gold-coated particles coated with DNA (includingthe transgene) shot into the transformable material. Techniques forgunning DNA into cells, tissue, explants, meristems, callus, embryos,and the like are well known in the prior art.

The DNA used for transformation of these plants clearly may be circular,linear, and double or single stranded.

Some of the time the DNA is in the form of a plasmid. The plasmid maycontain additional regulatory and/or targeting sequences which assistthe expression or targeting of the gene in the plant. The methods offorming plasmids for transformation are known in the art. Plasmidcomponents can include such items as: leader sequences, transitpolypeptides, promoters, terminators, genes, introns, marker genes, etc.The structures of the gene orientations can be sense, antisense, partialantisense or partial sense: multiple gene copies can be used.

After the transformation of the plant material is complete, the nextstep is identifying the cells or material, which has been transformed.In some cases, a screenable marker is employed such as thebeta-glucuronidase gene of the uidA locus of E. coli.

Then, the transformed cells expressing the colored protein are selectedfor either regeneration or further use. In many cases, a selectablemarker identifies the transformed material. The putatively transformedmaterial is exposed to a toxic agent at varying concentrations. Thecells not transformed with the selectable marker, which providesresistance to this toxic agent, die. Cells or tissues containing theresistant selectable marker generally proliferate. It has been notedthat although selectable markers protect the cells from some of thetoxic effects of the herbicide or antibiotic, the cells may still beslightly affected by the toxic agent by having slower growth rates. Ifthe transformed materials are cell lines then these lines are used toregenerate plants. The cells' lines are treated to induce tissuedifferentiation. Methods of regeneration of plants are well known in theart. General methods of culturing plant tissues are provided for exampleby Maki et al. “Procedures for Introducing Foreign DNA into Plants” inMethods in Plant Molecular Biology & Biotechnology, Glich et al. (Eds.pp. 67-88 CRC Press, 1993); and by Phillips et al. “Cell-Tissue Cultureand In-Vitro Manipulation” in Soybean & Soybean Improvement, 3rd EditionSprague et al. (Eds. pp. 345-387) American Society of Agronomy Inc. etal. 1988.

The plants from the transformation process or the plants resulting froma cross using a transformed line or the progeny of such plants whichcarry the transgene are transgenic plants.

The genes responsible for a specific gene trait are generally inheritedthrough the nucleus. Known exceptions are, e.g. the genes for malesterility, some of which are inherited cytoplasmically, but still act assingle gene traits. Male sterile soybean germplasm for hybrid soybeanproduction was taught in U.S. Pat. No. 4,648,204. In a preferredembodiment, a transgene to be introgressed into the cultivar AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104is integrated into the nuclear genome of the donor, non-recurrent parentor the transgene is directly transformed into the nuclear genome ofcultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104. In another embodiment of the invention, atransgene to be introgressed into cultivar AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104 isintegrated into the plastid genome of the donor, non-recurrent parent orthe transgene is directly transformed into the plastid genome ofcultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104. In a further embodiment of the invention, aplastid transgene comprises a gene that has transcribed from a singlepromoter, or two or more genes transcribed from a single promoter.

In another embodiment of the invention, DNA sequences native to soybeanas well as non-native DNA sequences can be transformed into the soybeancultivar of the invention and used to alter levels of native ornon-native proteins. Various promoters, targeting sequences, enhancingsequences, and other DNA sequences can be inserted into the genome forthe purpose of altering the expression of proteins. Reduction of theactivity of specific genes (also known as gene silencing or genesuppression) is desirable for several aspects of genetic engineering inplants.

Many techniques for gene silencing are well known to one of skill in theart, including but not limited to, knock-outs (such as by insertion of atransposable element such as mu (Vicki Chandler, The Maize Handbook Ch.118 (Springer-Verlag 1994)); antisense technology (see, e.g., Sheehy etal. (1988) PNAS USA 85:8805-8809; and U.S. Pat. Nos. 5,107,065;5,453,566; and 5,759,829); co-suppression (e.g., Taylor (1997) PlantCell 9:1245; Jorgensen (1990) Trends Biotech 8:340-344; Flavell (1994)PNAS USA 91:3490-3496; Finnegan et al. (1994) Bio/Technology 12:883-888;and Neuhuber et al. (1994) Mol Gen Genet 244:230-241); RNA interference(Napoli et al. (1990) Plant Cell 2:279-289; U.S. Pat. No. 5,034,323;Sharp (1999) Genes Dev 13:139-141; Zamore et al. (2000) Cell 101:25-33;and Montgomery et al. (1998) PNAS USA 95:15502-15507); virus-inducedgene silencing (Burton et al. (2000) Plant Cell 12:691-705; Baulcombe(1999) Curr Op Plant Biol 2:109-113); target-RNAspecific ribozymes(Flaselolf et al. (1988) Nature 334: 585-591); hairpin structures (Smithet al. (2000) Nature 407:319-320; WO99/53050; WO98/53083); microRNA(Aukerman & Sakai (2003) Plant Cell 15:2730-2741); ribozymes (Steineckeet al. (1992) EMBO J 11:1525; Perriman et al. (1993) Antisense Res Dev3:253); oligonucleotide mediated targeted modification (e.g.,WO03/076574 and WO99/25853); Zn-finger targeted molecules (e.g.,WO01/52620; WO03/048345; and WOOO/42219); use of exogenously applied RNA(e.g., US20110296556); and other methods or combinations of the abovemethods known to those of skill in the art.

A non-exclusive list of traits or nucleotide sequences capable of beingtransferred into cultivar AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104, for example by single locusconversion, using material and methods well known to those personsskilled in the art are as follows: genetic factor(s) responsible forresistance to brown stem rot (U.S. Pat. No. 5,689,035) or resistance tocyst nematodes (U.S. Pat. No. 5,491,081); a transgene encoding aninsecticidal protein, such as, for example, a crystal protein ofBacillus thuringiensis or a vegetative insecticidal protein fromBacillus cereus, such as VIP3 (see, for example, Estruch et al. NatBiotechnol [1997] 15:137-41); a herbicide tolerance transgene whoseexpression renders plants tolerant to the herbicide, for example,expression of an altered acetohydroxyacid synthase (AHAS) enzyme confersupon plants tolerance to various imidazolinone or sulfonamide herbicides(U.S. Pat. No. 4,761,373.) Other traits capable of being transformedinto cultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 include, for example, a non-transgenic traitconferring to cultivar AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 tolerance to imidazolinones orsulfonylurea herbicides; a transgene encoding a mutant acetolactatesynthase (ALS) that renders plants resistant to inhibition bysulfonylurea herbicides (U.S. Pat. No. 5,013,659); a gene encoding amutant glutamine synthetase (GS) resistant to inhibition by herbicidesthat are known to inhibit GS, e.g. phosphinothricin and methioninesulfoximine (U.S. Pat. No. 4,975,374); and a Streptomyces bar geneencoding a phosphinothricin acetyl transferase resulting in tolerance tothe herbicide phosphinothricin or glufosinate (U.S. Pat. No. 5,489,520.)Other genes capable of being transferred into the cultivar AR1403091,EE1600274, EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104of the invention include tolerance to inhibition by cyclohexanedione andaryloxyphenoxypropanoic acid herbicides (U.S. Pat. No. 5,162,602), whichis conferred by an altered acetyl coenzyme A carboxylase (ACCase);transgenic glyphosate tolerant plants, which tolerance is conferred byan altered 5-enolpyruvyl-3-phosphoshikimate (EPSP) synthase gene;tolerance to a protoporphyrinogen oxidase inhibitor, which is achievedby expression of a tolerant protoporphyrinogen oxidase enzyme in plants(U.S. Pat. No. 5,767,373.) Genes encoding altered protox resistant to aprotox inhibitor can also be used in plant cell transformation methods.For example, plants, plant tissue or plant cells transformed with atransgene can also be transformed with a gene encoding an altered protox(See U.S. Pat. No. 6,808,904 incorporated by reference) capable of beingexpressed by the plant. The thus-transformed cells are transferred tomedium containing the protox inhibitor wherein only the transformedcells will survive. Protox inhibitors contemplated to be particularlyuseful as selective agents are the diphenylethers (e.g. acifluorfen,5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobezoic acid; its methylester, or oxyfluorfen,2-chloro-1-(3-ethoxy-4-nitrophenoxy)-4-(trifluorobenzene)), oxidiazoles,(e.g. oxidiazon,3-[2,4-dichloro-5-(1-methylethoxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2-(3H)-one),cyclic imides (e.g. S-23142,N-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3,4,5,6-tetrahydrophthalimide;chlorophthalim, N-(4-chlorophenyl)-3,4,5,6-tetrahydrophthalimide),phenyl pyrazoles (e.g. TNPP-ethyl, ethyl2-[1-(2,3,4-trichlorophenyl)-4-nitropyrazolyl-5-oxy]propionate; M&B39279), pyridine derivatives (e.g. LS 82-556), and phenopylate and itsO-phenylpyrrolidino- and piperidinocarbamate analogs and bicyclictriazolones as disclosed in the International patent application WO92/04827; EP 532146).

The method is applicable to any plant cell capable of being transformedwith an altered protox-encoding gene, and can be used with any transgeneof interest. Expression of the transgene and the protox gene can bedriven by the same promoter functional on plant cells, or by separatepromoters.

Modified inhibitor-resistant protox enzymes of the present invention areresistant to herbicides that inhibit the naturally occurring protoxactivity. The herbicides that inhibit protox include many differentstructural classes of molecules (Duke et al., Weed Sci. 39: 465 (1991);Nandihalli et al., Pesticide Biochem. Physiol. 43: 193 (1992); Matringeet al., FEBS Lett. 245: 35 (1989); Yanase and Andoh, Pesticide Biochem.Physiol. 35: 70 (1989)), including the diphenylethers {e.g.acifluorifen, 5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobezoicacid; its methyl ester; or oxyfluorfen,2-chloro-1-(3-ethoxy-4-nitrophenoxy)-4-(trifluorobenzene)), oxidiazoles(e.g. oxidiazon,3-[2,4-dichloro-5-(1-methylethoxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2-(3H)-one),cyclic imides (e.g. S-23142,N-(4-chloro-2-fluoro-5-propargyloxyphenyl)-3,4,5,6-tetrahydrophthalimide;chlorophthalim, N-(4-chlorophenyl)-3,4,5,6-tetrahydrophthalimide),phenyl pyrazoles (e.g. TNPP-ethyl, ethyl2-[1-(2,3,4-trichlorophenyl)-4-nitropyrazolyl-5-oxy]propionate; M&B39279), pyridine derivatives (e.g. LS 82-556), and phenopylate and itsO-phenylpyrrolidino- and piperidinocarbamate analogs.

Direct selection may be applied where the trait acts as a dominanttrait. An example of a dominant trait is herbicide tolerance. For thisselection process, the progeny of the initial cross are sprayed with theherbicide prior to the backcrossing. The spraying eliminates any plantthat does not have the desired herbicide tolerance characteristic, andonly those plants that have the herbicide tolerance gene are used in thesubsequent backcross. This process is then repeated for the additionalbackcross generations.

In yet another embodiment of the present invention, a transgenetransformed or introgressed into cultivar AR1403091, EE1600274,EE1600891, EE1660258, EE1760174, EE1760847, and/or EE1761104, forexample as a single locus conversion, comprises a gene conferringtolerance to a herbicide and at least another nucleotide sequence foranother trait, such as for example, insect resistance or tolerance toanother herbicide. Another gene capable of being transferred into thecultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 of the invention expresses thioredoxin andthioredoxin reductase enzymes for modifying grain digestibility andnutrient availability (U.S. Pat. Appl. No. 20030145347.) Furtherreproduction of the cultivar can occur by tissue culture andregeneration.

Tissue culture of various tissues of soybeans and regeneration of plantstherefrom is well known and widely published. For example, reference maybe had to Komatsuda, T. et al., “Genotype X Sucrose Interactions forSomatic Embryogenesis in Soybean,” Crop Sci. 31:333-337 (1991);Stephens, P. A. et al., “Agronomic Evaluation of Tissue-Culture-DerivedSoybean Plants,” Theor. Appl. Genet. (1991) 82:633-635; Komatsuda, T. etal., “Maturation and Germination of Somatic Embryos as Affected bySucrose and Plant Growth Regulators in Soybeans Glycine gracilis Skvortzand Glycine max (L.) Merr.,” Plant Cell, Tissue and Organ Culture,28:103-113 (1992); Dhir, S. et al., “Regeneration of Fertile Plants fromProtoplasts of Soybean (Glycine max L. Merr.): Genotypic Differences inCulture Response,” Plant Cell Reports (1992) 11:285-289; Pandey, P. etal., “Plant Regeneration from Leaf and Hypocotyl Explants of Glycinewightii (W. and A.) VERDC. var longicauda,” Japan J. Breed. 42:1-5(1992); and Shetty, K., et al., “Stimulation of In Vitro ShootOrganogenesis in Glycine max (Merrill.) by Allantoin and Amides,” PlantScience 81:(1992) 245-251; as well as U.S. Pat. No. 5,024,944, issuedJun. 18, 1991 to Collins et al. and U.S. Pat. No. 5,008,200, issued Apr.16, 1991 to Ranch et al. Thus, another aspect of this invention is toprovide cells that upon growth and differentiation produce soybeanplants having all or essentially all the physiological and morphologicalcharacteristics of cultivar AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104. The disclosures, publications,and patents that are disclosed herein are all hereby incorporated hereinin their entirety by reference.

Sublines of soybean variety AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 may also be developed and areprovided. Although soybean variety AR1403091, EE1600274, EE1600891,EE1660258, EE1760174, EE1760847, and/or EE1761104 contains substantiallyfixed genetics and is phenotypically uniform with no off types expected,there still remains a small proportion of segregating loci either withinindividuals or within the population as a whole. Sublining provides theability to select for these loci, which have no apparent morphologicalor phenotypic effect on the plant characteristics, but may have aneffect on overall yield. For example, the methods described in U.S. Pat.Nos. 5,437,697, 7,973,212, and US2011/0258733, and US2011/0283425 (eachof which is herein incorporated by reference) may be utilized by abreeder of ordinary skill in the art to identify genetic loci that areassociated with yield potential to further purify the variety in orderto increase its yield. A breeder of ordinary skill in the art may fixagronomically relevant loci by making them homozygous in order tooptimize the performance of the variety. The development of soybeansublines and the use of accelerated yield technology is a plant breedingtechnique.

The seed of soybean cultivar AR1403091, EE1600274, EE1600891, EE1660258,EE1760174, EE1760847, and/or EE1761104 further comprising one or morespecific, single gene traits, the plant produced from the seed, thehybrid soybean plant produced from the crossing of the cultivar with anyother soybean plant, hybrid seed, and various parts of the hybridsoybean plant can be utilized for human food, livestock feed, and as araw material in industry.

Soybean is the world's leading source of vegetable oil and protein meal.The oil extracted from soybeans is used for cooking oil, margarine, andsalad dressings. Soybean oil is composed of saturated, monounsaturatedand polyunsaturated fatty acids. It has a typical composition of 11%palmitic, 4% stearic, 25% oleic, 50% linoleic and 9% linolenic fattyacid content (“Economic Implications of Modified Soybean Traits SummaryReport”, Iowa Soybean Promotion Board & American Soybean AssociationSpecial Report 92S, May 1990.) Changes in fatty acid composition forimproved oxidative stability and nutrition are constantly sought after.(U.S. Pat. No. 5,714,670 Soybeans Having Low Linolenic Acid and LowPalmitic Acid Contents; U.S. Pat. No. 5,763,745 Soybeans Having LowLinolenic Acid Content and Palmitic Acid Content of at Least ElevenPercent; U.S. Pat. No. 5,714,668 Soybeans Having Low Linolenic Acid AndElevated Stearic Acid Content; U.S. Pat. No. 5,714,669 A17 SoybeansHaving Low Linolenic Acid Content and Descendents; U.S. Pat. No.5,710,369 A16 Soybeans Having Low Linolenic Acid Content andDescendents; U.S. Pat. No. 5,534,425 Soybeans Having Low Linolenic AcidContent and Method of Production; U.S. Pat. No. 5,7508,44 SoybeansCapable of Forming a Vegetable Oil Having Specified Concentrations ofPalmitic and Stearic Acids; U.S. Pat. No. 5,750,845 Soybeans Capable ofForming a Vegetable Oil Having a Low Saturated Fatty Acid Content; U.S.Pat. No. 5,585,535 Soybeans and Soybean Products Having Low PalmiticAcid Content; U.S. Pat. No. 5,850,029 Soybean Designated AX7017-1-3;U.S. Pat. No. 5,663,485 Soybean Designated A89-259098; U.S. Pat. No.5,684,230 Soybean Designated AX 4663-5-4-5; U.S. Pat. No. 5,684,231Soybean Designated A1937 NMU-85; U.S. Pat. No. 5,714,672 SoybeanDesignated ElginEMS-421; U.S. Pat. No. 5,602,311 Soybeans and SoybeanProducts Having High Palmitic Acid Content; U.S. Pat. No. 5,795,969Soybean Vegetable Oil Having Elevated Concentrations of Both Palmiticand Stearic Acid; U.S. Pat. No. 5,557,037 Soybeans Having ElevatedContents of Saturated Fatty Acids; U.S. Pat. No. 5,516,980 SoybeanVariety XB37ZA; U.S. Pat. No. 5,530,183 Soybean Variety 9253; U.S. Pat.No. 5,750,846 Elevated Palmitic Acid Production in Soybeans; U.S. Pat.No. 6,060,647 Elevated Palmitic Acid Production in Soybeans; U.S. Pat.No. 6,025,509 Elevated Palmitic Acid Production in Soybeans; U.S. Pat.No. 6,133,509 Reduced Linolenic Acid Production in Soybeans; U.S. Pat.No. 5,986,118 Soybean Vegetable Oil Possessing a Reduced Linolenic AcidContent; U.S. Pat. No. 5,850,030 Reduced Linolenic Acid Production inSoybeans). Industrial uses of soybean oil that is subjected to furtherprocessing include ingredients for paints, plastics, fibers, detergents,cosmetics, and lubricants. Soybean oil may be split, inter-esterified,sulfurized, epoxidized, polymerized, ethoxylated, or cleaved. Designingand producing soybean oil derivatives with improved functionality,oliochemistry is a rapidly growing field. The typical mixture oftriglycerides is usually split and separated into pure fatty acids,which are then combined with petroleum-derived alcohols or acids,nitrogen, sulfonates, chlorine, or with fatty alcohols derived from fatsand oils.

The techniques of seed treatment application are well known to thoseskilled in the art, and they may be used readily in the context of thepresent invention. The seed treating compositions can be applied to theseed as slurry, mist or a soak or other means know to those skilled inthe art of seed treatment. Seed treatments may also be applied by othermethods, e.g., film coating or encapsulation. The coating processes arewell known in the art, and employ, for seeds, the techniques of filmcoating or encapsulation, or for the other multiplication products, thetechniques of immersion. Needless to say, the method of application ofthe compositions to the seed may be varied and is intended to includeany technique that is to be used.

The term “fungicide” as utilized herein is intended to cover compoundsactive against phytopathogenic fungi that may belong to a very widerange of compound classes. Examples of compound classes to which thesuitable fungicidally active compound may belong include both roomtemperature (25.degree. C.) solid and room temperature liquid fungicidessuch as: triazole derivatives, strobilurins, carbamates (including thio-and dithiocarbamates), benzimidazoles (thiabendazole),N-trihalomethylthio compounds (captan), substituted benzenes,carboxamides, phenylamides and phenylpyrroles, and mixtures thereof.

The present invention includes a method for preventing damage by a pestto a seed of the present invention and/or shoots and foliage of a plantgrown from the seed of the present invention. Broadly the methodincludes treating the seed of the present invention with a pesticide.The pesticide is a composition that stops pests including insects,diseases, and the like. Broadly compositions for seed treatment caninclude but is not limited to any of one of the following: aninsecticide, or a fungicide.

The method comprises treating an unsown seed of the present inventionwith neonicotinoid composition. One of these compositions isthiamethoxam. Additionally, the neonicotinoid composition can include atleast one pyrethrin or synthetic pyrethroid, to reduce pest damage. Morespecifically there is a method of seed treatment which employsthiamethoxam and at least one pyrethrin or pyrethroid are comprisedwithin a seed coating treated on the seed of the present invention. Thecombination, if thiamethoxam is employed, can be coated at a rate whichis greater than 200 gm/100 kg of seed. The method includes having atleast one of the pyrethroids being a systemic insecticide.

The pyrethrin or synthetic pyrethroid, if employed can be selected fromthe group consisting of taufluvalinate, flumethrin, trans-cyfluthrin,kadethrin, bioresmethrin, tetramethrin, phenothrin, empenthrin,cyphenothrin, prallethrin, imiprothrin, allethrin and bioallethrin.

The fungicidally active compounds and/or the insecticidal activecompounds are employed in a fungicidally and/or insecticidally effectiveamount in the composition. Mixtures of one or more of the followingactive compounds are usable as an active component treatment of the seedof the present invention. Examples of suitable individual compounds foruse in seed treatments are listed below. Where known, the common name isused to designate the individual compounds (q.v. the Pesticide Manual,12th edition, 2001, British Crop Protection Council).

Suitable triazole derivatives include propiconazole, difenconazole,tebuconazole, tetraconazole and triticonazole. Suitable strobilurinsinclude trifloxystrobin, azoxystrobin, kresoxim-methyl andpicoxystrobin. Suitable carbamates include thiram. Suitable substitutedbenzenes include PCNB and chlorothalonil. Suitable carboxamides includecarboxin. Specific phenylamides usable in the compositions and methodsinclude metalaxyl. A specific phenylpyrrole usable in the composition isfludioxonil.

Other suitable fungicidal compounds that maybe mentioned are Benomyl(also known as Benlate), Bitertanol, Carbendazim, Capropamid, Cymoxanil,Cyprodinil, Ethirimol, Fenpiclonil, Fenpropimorph, Fluquinconazole,Flutolanil, Flutriafol, Fosetyl-aluminum, Fuberidazole, Guazatine,Hymexanol, Kasugamycin, Imazalil, Imibenconazole,Iminoctadine-triacetate, Ipconazole, Iprodione, Mancozeb, Maneb,Mepronil, Metalaxyl, Metalaxyl-M (Mefenoxam), Metconazole, Metiram, MON65500 (Silthiopham-ISO proposed), Myclobutanil, Nuarimol, Oxadixyl,Oxine-copper, Oxolinic acid, Pefurazoate, Pencycuron, Prochloraz,Propamocarb hydrochloride, Pyroquilon, Silthiopham—see MON 65500,Tecnazene, Thifluzamide, Thiophenate-methyl, Tolclofos-methyl,Triadimenol, Triazoxide and Triflumizole.

The fungicidally active compounds and/or the insecticidal activecompounds are employed in a fungicidally and/or insecticidally effectiveamount in the composition. Mixtures of one or more of the followingactive compounds also are usable as an active component treatment of theseed of the present invention.

In one seed treatment, mixtures of at least one ambient liquid fungicide(for example, a phenylamide such as R-metalaxyl) and at least oneambient solid fungicide (for example, a phenylpyrrole such asfludioxonil) could be employed. The apparatus for providing theappropriate amount of seed treatment of a specific chemical compositionfor a seed are well known in the seed coating industry (See, forexample, U.S. Pat. Nos. 5,632,819 and 5,891,246).

Soybean seeds, plants, and plant parts may be used or processed forfood, animal feed, or a raw material(s) for industry. Soybean is notjust a seed it is also used as a grain. Soybean is widely used as asource of protein for animal feeds for poultry, swine and cattle. Thesoybean grain is a commodity. The soybean commodity plant productsinclude but are not limited to protein concentrate, protein isolate,soybean hulls, meal, flower, oil and the whole soybean itself. Soybeanseeds can be crushed, or a component of the seeds can be extracted inorder to make a plant product, such as protein concentrate, proteinisolate, soybean hulls, meal, flour, or oil for a food or feed product.Methods of producing a plant product, such as protein concentrate,protein isolate, soybean hulls, meal, flour, or oil for a food or feedproduct are provided. Also provided are the protein concentrate, proteinisolate, soybean hulls, meal, flour, or oil produced by the methods.

Oil extracted from soybeans is used for cooking oil, margarine, andsalad dressings. Soybean oil has a typical composition of 11% palmitic,4% stearic, 25% oleic, 50% linoleic, and 9% linolenic fatty acidcontent. Industrial uses of soybean oil, which is typically subjected tofurther processing, include ingredients for paints, plastics, fibers,detergents, cosmetics, lubricants, and biodiesel fuel. Soybean oil maybe split, inter-esterified, sulfurized, epoxidized, polymerized,ethoxylated, or cleaved. To produce oil, the harvested soybeans arecracked, adjusted for moisture content, rolled into flakes, and then theoil is solvent-extracted. The oil extract is refined, optionally blendedand/or hydrogenated. Some soybean varieties have modified fatty acidprofiles and can be used to produce soybean oil with a modified fattyacid composition. Oil with 3% or less linolenic acid is classified aslow linolenic oil, oil with less than 1% linolenic acid is classified asultra low linolenic oil. Oil with 70% or higher of oleic acid isclassified as high oleic oil.

Soybeans are also used as a food source for both animals and humans.Soybeans are widely used as a source of protein for animal feed. Thefibrous hull is removed from whole soybean and the oil is extracted. Theremaining meal is a combination of carbohydrates and approximately 50%protein. This remaining meal is heat treated under well-establishedconditions and ground in a hammer mill. Soybean is a predominant sourcefor livestock feed components. In addition to soybean meal, soybean canbe used to produce soy flour. Soy flour refers to defatted soybeanswhere special care was taken during desolventizing to minimize proteindenaturation and to retain a high nitrogen solubility index (NSI) inmaking the flour. Soy flour is the typical starting material forproduction of soy concentrate and soy protein isolate. Defatted soyflour is obtained from solvent extracted flakes, and contains less than1% oil. Full-fat soy flour is made from whole beans and contains about18% to 20% oil. Low-fat soy flour is made by adding back some oil todefatted soy flour. The lipid content varies, but is usually between4.5-9%. High-fat soy flour can also be produced by adding soybean oil todefatted flour at the level of 15%. Lecithinated soy flour is made byadding soybean lecithin to defatted, low-fat or high-fat soy flours toincrease dispersibility and impart emulsifying properties.

For human consumption, soybean can be used to produce edible ingredientswhich serve as an alternative source of dietary protein. Common examplesinclude milk, cheese, and meat substitutes. Additionally, soybean can beused to produce various types of fillers for meat and poultry products.Vitamins and/or minerals may be added to make soy products nutritionallymore equivalent to animal protein sources as the protein quality isalready roughly equivalent.

Deposit Information

Applicants have made a deposit of at least 2500 seeds of soybeancultivar AR1403091, EE1600274, EE1600891, EE1660258, EE1760174,EE1760847, and/or EE1761104 with the American Type Culture Collection(ATCC) Patent Depository, 10801 University Blvd., Manassas, VA 20110.The ATCC numbers of the deposits are PTA-126546, PTA-126547, PTA-126545,PTA-126551, PTA-126552, ______, and PTA-126553, respectively. The dateof deposit was Dec. 19, 2019 for PTA-126551, PTA-126552, and PTA-126553and Dec. 13, 2019 for PTA-126546, PTA-126547, and PTA-126545, and theseed was tested on Jan. 9, 2020 for PTA-126545, PTA-126551, andPTA-126552 and on Jan. 27, 2020 for PTA-126546, PTA-126553, andPTA-126547 and all were found to be viable. Access to this deposit willbe available during the pendency of the application to the Commissionerfor patents and persons determined by the Commissioner to be entitledthereto upon request. Upon granting of a patent on any claims in theapplication, the Applicants will make the deposit available to thepublic pursuant to 37 CFR § 1.808. Additionally, Applicants will meetthe requirements of 37 CFR § 1.801-1.809, including providing anindication of the viability of the sample when the deposit is made. TheATCC deposit will be maintained in that depository, which is a publicdepository, for a period of 30 years, or 5 years after the last request,or for the enforceable life of the patent, whichever is longer, and willbe replaced if it becomes nonviable during that period.

AR1403091

AR1403091 is employed in a number of plot repetitions to establish traitcharacteristics.

AR1403091 is a novel soybean cultivar with high yield potential. Theinvention relates in part to seeds of the cultivar AR1403091, plants ofthe cultivar AR1403091 and to methods for producing a soybean plantproduced by crossing the soybean cultivar AR1403091 by itself or toanother soybean genotype.

AR1403091 is a Group 2 Maturity soybean cultivar. This variety has an RMof 2.500. To be sold commercially in Ontario, Canada in areas whereearly mid group 2 maturity soybeans are grown. Specific area where bestadaptation occurs includes: Ontario, Canada. The target for this varietyis geographic areas that grow mid Group 2 maturity, conventionalherbicide varieties that require Soybean Cyst Nematode resistance.

The characteristics and traits of AR1403091 are listed below.

TABLE 1 CHARACTERISTICS AND TRAITS Herbicide Transgene Insect TransgeneOther Transgene Relative 2.500 Maturity Sulfonylurea N Seed ShapeHypocotyl Tolerance Color Metribuzin Toler Seed Coat Luster Plant PTTIyTolerance Morphological Aphid Gene Rag1_S Peroxidase Leaf Color %Protein @ Seed Size g/100 seeds Leaf Shape 13% mst Calculated % Oil @13%mst Growth Habit INDET Leaf Shape Plant Health Phytophthora Gene S StemCanker Tolerance Rust Gene Chloride Sensitivity CLMS SCN Res 88788RootKnot Nematode Sting Source Nematode R1 R2 R3 R5 R7 R9 R14 IncognitaArenaria Javanica Pratylenchus FI % FI % FI % FI % FI % FI % FI % SCN =Soybean Cyst Nematode, RKN= Root Knot Nematode Rps gene indicates thespecific gene for resistance but if none are indicated then none areknown to be present. % Protein and % Oil are given at 13% moisture(standard moisture). MON89788 indicates this variety carries theglyphosate tolerance transgene derived from event MON 89788; MON87708indicates this variety carries the dicamba tolerance transgene derivedfrom event MON 87708. Seed shape: 1 = spherical; 2 =spherical-flattened; 3 = elongate; 4 = elongate-flattened Seed coatluster: 1 = dull; 2 = shiny Plant Morphological traits are listed in theorder of flower, pubescence, pod color, and hilum. For flower, P =purple, W = white, and S = segregating (mixture of colors). Forpubescence, G = gray, T = tawny, Lt = LT = light tawny, LBr = LB = lightbrown, and S = segregating (mixture of colors). For pod color, T = tan,B = brown, LBr = light brown, and S = segregating (mixture of colors).For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF = Bf =buff, BL = Bl = black, IB = Ib = imperfect black, Y = yellow, IY = Iy =imperfect yellow, S = segregating (mixture of colors). Leaf Color: 1 =light green; 2 = medium green; 3 = dark green Ratings are on a 1 to 9scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 2 Agronomic and Disease Traits Hrvst Grn Mat Grn VHNO Yield EmergeLod Lod Days Height Canopy Branch Stem PRTNP S29-R5X 72.4 2.8 5.0 1.0124.9 34.4 5.5 5.0 1.9 39.5 S21-C3 68.9 2.3 2.5 1.0 117.7 38.0 4.5 3.51.6 42.8 S16-F5 55.2 2.8 1.0 1.0 114.5 31.9 5.5 3.5 1.1 43.7 S20-M1 63.82.5 1.5 2.5 116.4 39.4 5.0 4.0 1.2 43.3 S20-G7 58.8 3.0 1.0 1.0 115.034.4 4.5 3.0 1.4 43.1 S18-R6 57.2 3.0 1.0 1.0 113.8 33.7 3.5 2.5 1.339.9 AR1403091 62.1 3.0 1.0 1.5 122.2 39.0 6.0 5.5 2.1 32.7 Environments7.0 2.0 1.0 1.0 5.0 1.0 1.0 1.0 5.0 1.0 Grand 61.7 2.6 2.9 2.0 117.435.2 5.0 3.9 2.1 42.5 Mean Check 61.4 2.5 3.2 2.1 116.8 35.0 4.8 3.7 2.142.4 Mean LSD (0.05) 4.6 0.8 1.6 0.0 3.0 0.0 0.0 1.6 1.6 1.9 OIL_ DPS_FELS PM_ BP_ TSP_ VHNO P R R R PRR R RUSTR SDS SWM R S29-R5X 22.9 2.5#N/A #N/A 3.5 #N/A #N/A 1.0 3.0 #N/A S21-C3 20.7 5.3 #N/A #N/A 6.5 #N/A#N/A 2.5 5.0 #N/A S16-F5 20.9 5.0 #N/A #N/A 6.0 #N/A #N/A 2.0 2.5 #N/AS20-M1 20.7 6.3 #N/A #N/A 4.5 #N/A #N/A 3.0 4.5 #N/A S20-G7 21.5 3.8#N/A #N/A 4.5 #N/A #N/A 8.0 1.5 #N/A S18-R6 22.2 3.5 #N/A #N/A 6.0 #N/A#N/A 3.0 1.5 #N/A AR1403091 19.6 3.5 #N/A #N/A 5.5 #N/A #N/A 2.0 3.0#N/A Environments 1.0 2.0 #N/A #N/A 1.0 #N/A #N/A 1.0 1.0 #N/A Grand21.3 4.5 #N/A #N/A 5.0 #N/A #N/A 4.2 2.5 #N/A Mean Check 21.5 4.7 #N/A#N/A 5.0 #N/A #N/A 4.4 2.5 #N/A Mean LSD (0.05) 1.0 1.8 #N/A #N/A 0.0#N/A #N/A 2.2 1.8 #N/A #N/A = no data available

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from AR1403091.AR1403091 yields more than S16-F5 and S18-R6, similar to S20-G7 andS20-M1 and less than S21-C3 (LSD 0.05-4.6 bu/a). AR1403091 is later inmaturity when compared to S18-R6, S20-G7, S20-M1, S21-C3 and S16-F5 (LSD0.05=3.0). AR1403091 is similar in protein content when compared toS20-G7, S20-M1, S16-F5, and S21-C3 and higher in protein content thanS18-R6 (LSD 0.05-1.9). AR1403091 can be differentiated from S21-C3,S16-F5, and S20-M1 since AR1403091 has tawny pubescence, tan pod wall,Imperfect yellow hilum, and no genes for phytophthora resistance.S21-C3, S16-F5, and S20-M1 have gray pubescence, tan pod wall, yellowhilum, and the Rps1c gene for phytophthora resistance. S18-R6 has graypubescence, tan pod wall, yellow hilum, and the Rps1a gene forphytophthora resistance. S20-G7 has gray pubescence, brown pod wall,yellow hilum, and the Rps1c gene for phytophthora resistance

EE1600274

EE1600274 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1600274 is a novel soybean cultivar with high yield potential. Theinvention relates in part to seeds of the cultivar EE1600274, plants ofthe cultivar EE1600274 and to methods for producing a soybean plantproduced by crossing the soybean cultivar EE1600274 by itself or toanother soybean genotype.

EE1600274 is a Group 0 Maturity soybean cultivar. This variety has an RMof 0.400. To be sold commercially in Quebec and Ontario, Canada in areaswhere mid Group 0 maturity soybeans are grown. Specific area where bestadaptation occurs includes: Quebec, and Ontario, Canada. The target forthis variety is geographic areas that grow mid Group 0 maturity,conventional herbicide varieties that require Soybean Cyst Nematoderesistance.

The characteristics and traits of EE1600274 are listed below.

TABLE 3 CHARACTERISTICS AND TRAITS Herbicide Transgene Insect TransgeneOther Transgene Relative 0.400 Maturity Sulfonylurea Tolerance N SeedShape Hypocotyl Color Metribuzin Tolerance Toler Seed Coat Luster PlantPGTY Morphological Aphid Gene Rag1_S Peroxidase Leaf Color % Protein @13% mst Seed Size g/ Leaf Shape 100 seeds Calculated % Oil (@13% mstGrowth Habit INDET Leaf Shape Plant Health Phytophthora Gene Rps1c StemCanker Tolerance Rust Gene Chloride Sensitivity CLMS SCN Res 88788RootKnot Nematode Sting Nematode Source R1 R2 R3 R5 R7 R9 R14 IncognitaArenaria Javanica Pratylenchus FI % FI % FI % FI % FI % FI % FI % SCN =Soybean Cyst Nematode, RKN = Root Knot Nematode Rps gene indicates thespecific gene for resistance but if none are indicated then none areknown to be present. % Protein and % Oil are given at 13% moisture(standard moisture). MON89788 indicates this variety carries theglyphosate tolerance transgene derived from event MON 89788; MON87708indicates this variety carries the dicamba tolerance transgene derivedfrom event MON 87708. Seed shape: 1 = spherical; 2 =spherical-flattened; 3 = elongate; 4 = elongate-flattened Seed coatluster: 1 = dull; 2 = shiny Plant Morphological traits are listed in theorder of flower, pubescence, pod color, and hilum. For flower, P =purple, W = white, and S = segregating (mixture of colors). Forpubescence, G = gray, T = tawny, Lt = LT= light tawny, LBr = LB = lightbrown, and S = segregating (mixture of colors). For pod color, T = tan,B = brown, LBr = light brown, and S = segregating (mixture of colors).For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF = Bf =buff, BL = Bl = black, IB = Ib = imperfect black, Y = yellow, IY = Iy =imperfect yellow, S = segregating (mixture of colors). Leaf Color: 1 =light green; 2 = medium green; 3 = dark green Ratings are on a 1 to 9scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 4 Agronomic and Disease Traits Hryst Grn Mat OIL_ VHNO YieldEmerge Lod Lod Days Height Canopy Branch PRTNP P Emperor 62.1 2.5 1.51.7 120.2 35.4 5.8 5.5 44.3 20.8 Ezra 61.9 3.3 3.0 1.8 116.8 33.5 3.83.0 39.1 22.9 S07-D2 55.6 2.7 3.5 2.8 114.2 37.4 4.5 4.0 45.1 19.4S10-R2 60.7 3.0 2.0 5.6 115.2 36.8 5.0 6.0 44.8 19.8 S03-W4 54.3 3.0 1.03.2 113.6 33.5 3.1 3.0 43.4 22.1 S07-M8 59.2 3.2 1.0 1.3 116.5 33.9 4.34.0 44.7 20.7 EE1600274 55.1 3.3 1.5 3.1 115.6 30.3 4.8 5.0 46.0 20.1Environments 9.0 3.0 1.0 3.0 5.0 1.0 2.0 1.0 1.0 1.0 Grand 57.3 3.1 1.63.2 115.5 34.1 4.5 4.0 43.2 21.3 Mean Check 57.9 3.0 1.8 2.9 115.2 34.14.6 4.1 42.8 21.3 Mean LSD (0.05) 3.9 1.0 0.0 2.4 2.0 3.3 1.1 1.5 0.70.5 DPS_ PM_ BP_ SDS_ SCL_ TSP_ VHNO R SBSSN FELSR R PRR R RUSTR R R REmperor 2.3 1733.0 #N/A #N/A 4.0 #N/A #N/A #N/A #N/A #N/A Ezra 3.52185.5 #N/A #N/A 5.0 #N/A #N/A #N/A #N/A #N/A S07-D2 8.3 1990.5 #N/A#N/A 3.5 #N/A #N/A #N/A #N/A #N/A S10-R2 8.3 1981.5 #N/A #N/A 6.5 #N/A#N/A #N/A #N/A #N/A S03-W4 3.7 2209.5 #N/A #N/A 5.5 #N/A #N/A #N/A #N/A#N/A S07-M8 4.3 1930.0 #N/A #N/A 4.5 #N/A #N/A #N/A #N/A #N/A EE16002745.7 1836.0 #N/A #N/A 6.5 #N/A #N/A #N/A #N/A #N/A Environments 3.0 1.0#N/A #N/A 1.0 #N/A #N/A #N/A #N/A #N/A Grand 5.0 2029.7 #N/A #N/A 5.0#N/A #N/A #N/A #N/A #N/A Mean Check 5.4 2074.0 #N/A #N/A 4.8 #N/A #N/A#N/A #N/A #N/A Mean LSD (0.05) 1.5 100.1 #N/A #N/A 0.0 #N/A #N/A #N/A#N/A #N/A #N/A = no data available

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1600274.EE1600274 yields similar to S03-W4 and S07-D2 and less than S07-M8 andS10-R2 (LSD 0.05=3.9 bu/a). EE1600274 is similar in maturity to S03-W4,S07-M8, S07-D2 and S10-R2 (LSD 0.05=2.0). EE1600274 is similar in heightto S03-W4 and shorter than S07-M8, S07-D2 and S10-R2 (LSD 0.05-3.3).EE1600274 is similar in protein content to S07-D2 and higher thanS03-W4, S07-M8, and S10-R2 (LSD 0.05=0.7). EE1600274 can bedifferentiated from S10-R2 since EE1600274 has gray pubescence, tan podwall, yellow hilum, the Rps1c gene for phytophthora resistance and thesoybean cyst nematode resistance gene P188788. S10-R2 has graypubescence, tan pod wall, yellow hilum, no gene for phytophthoraresistance and the soybean cyst nematode resistance gene P188788. S07-D2has gray pubescence, brown pod wall, yellow hilum, the Rps3a gene forphytophthora resistance, and no soybean cyst nematode resistance genes.S07-M8 has light tawny pubescence, brown pod wall, Imperfect yellowhilum, the Rps1c gene for phytophthora resistance and no soybean cystnematode resistance genes. S03-W4 has tawny pubescence, brown pod wall,Imperfect yellow hilum, the Rps1c gene for phytophthora resistance andno soybean cyst nematode resistance genes.

EE1600891

EE1600891 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1600891 is a novel soybean cultivar with high yield potential. Theinvention relates in part to seeds of the cultivar EE1600891, plants ofthe cultivar EE1600891 and to methods for producing a soybean plantproduced by crossing the soybean cultivar EE1600891 by itself or toanother soybean genotype.

EE1600891 is a Group 2 Maturity soybean cultivar. This variety has an RMof 2.100. To be sold commercially in Ontario, Canada in areas whereearly Group 2 maturity soybeans are grown. Specific area where bestadaptation occurs includes: Ontario, Canada. The target for this varietyis geographic areas that grow early Group 2 maturity, conventionalherbicide varieties that require Soybean Cyst Nematode resistance.

The characteristics and traits of EE1600891 are listed below.

TABLE 5 CHARACTERISTICS AND TRAITS Herbicide Transgene Insect TransgeneOther Transgene Relative 2.100 Maturity Sulfonylurea Tolerance N SeedShape Hypocotył Color Metribuzin Tolerance Toler Seed Coat Luster PlantPGTY Morphological Aphid Gene Rag1_S Peroxidase Leat Color % Protein @13% mst Seed Size g/ Leaf Shape 100 seeds Calculated % Oil @13% mstGrowth Habit INDET Leaf Shape Plant Health Phytophthora Gene S StemCanker Tolerance Rust Gene Chloride Sensitivity CLMS SCN Res 88788RootKnot Nematode Sting Source Nematode R1 R2 R3 R5 R7 R9 R14 IncognitaArenaria Javanica Pratylenchus FI % FI % FI % FI % FI % FI % FI % SCN =Soybean Cyst Nematode, RKN = Root Knot Nematode Rps gene indicates thespecific gene for resistance but if none are indicated then none areknown to be present. % Protein and % Oil are given at 13% moisture(standard moisture). MON89788 indicates this variety carries theglyphosate tolerance transgene derived from event MON 89788; MON87708indicates this variety carries the dicamba tolerance transgene derivedfrom event MON 87708. Seed shape: 1 = spherical; 2 =spherical-flattened; 3 = elongate; 4 = elongate-flattened Seed coatluster: 1 = dull; 2 = shiny Plant Morphological traits are listed in theorder of flower, pubescence, pod color, and hilum. For flower, P =purple, W = white, and S = segregating (mixture of colors). Forpubescence, G = gray, T = tawny, Lt = LT = light tawny, LBr = LB = lightbrown, and S = segregating (mixture of colors). For pod color, T = tan,B = brown, LBr = light brown, and S = segregating (mixture of colors).For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF = Bf =buff, BL = Bl = black, IB = Ib = imperfect black, Y= yellow, IY = Iy =imperfect yellow, S = segregating (mixture of colors). Leaf Color: 1 =light green; 2 = medium green; 3 = dark green Ratings are on a 1 to 9scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 6 Agronomic and Disease Traits Hrvst Grn Mat Grn VHNO Yield EmergeLod Lod Days Height Canopy Branch Stem PRTNP S29-R5X 72.4 2.8 5.0 1.0124.9 34.4 5.5 5.0 1.9 39.5 S21-03 68.9 2.3 2.5 1.0 117.7 38.0 4.5 3.51.6 42.8 S16-F5 55.2 2.8 1.0 1.0 114.5 31.9 5.5 3.5 1.1 43.7 S20-M1 63.82.5 1.5 2.5 116.4 39.4 5.0 4.0 1.2 43.3 S20-G7 58.8 3.0 1.0 1.0 115.034.4 4.5 3.0 1.4 43.1 S18-R6 57.2 3.0 1.0 1.0 113.8 33.7 3.5 2.5 1.339.9 EE1600891 61.5 3.0 1.0 3.0 118.7 38.4 7.0 5.0 2.6 46.8 Environments7.0 2.0 1.0 1.0 5.0 1.0 1.0 1.0 5.0 1.0 Grand 61.7 2.6 2.9 2.0 117.435.2 5.0 3.9 2.1 42.5 Mean Check 61.4 2.5 3.2 2.1 116.8 35.0 4.8 3.7 2.142.4 Mean LSD (0.05) 4.6 0.8 1.6 0.0 3.0 0.0 0.0 1.6 1.6 1.9 OIL_ DPS_PM_ PR BP_ TSP_ VHNO P R FELSR R R R RUSTR SDS SWM R S29-R5X 22.9 2.5#N/A #N/A 3.5 #N/A #N/A 1.0 3.0 #N/A S21-03 20.7 5.3 #N/A #N/A 6.5 #N/A#N/A 2.5 5.0 #N/A S16-F5 20.9 5.0 #N/A #N/A 6.0 #N/A #N/A 2.0 2.5 #N/AS20-M1 20.7 6.3 #N/A #N/A 4.5 #N/A #N/A 3.0 4.5 #N/A S20-G7 21.5 3.8#N/A #N/A 4.5 #N/A #N/A 8.0 1.5 #N/A S18-R6 22.2 3.5 #N/A #N/A 6.0 #N/A#N/A 3.0 1.5 #N/A EE1600891 19.2 4.0 #N/A #N/A 5.5 #N/A #N/A 4.5 4.0#N/A Environments 1.0 2.0 #N/A #N/A 1.0 #N/A #N/A 1.0 1.0 #N/A Grand21.3 4.5 #N/A #N/A 5.0 #N/A #N/A 4.2 2.6 #N/A Mean Check 21.5 4.7 #N/A#N/A 5.0 #N/A #N/A 4.4 2.5 #N/A Mean LSD (0.05) 1.0 1.8 #N/A #N/A 0.0#N/A #N/A 2.2 1.8 #N/A

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1600891.EE1600891 yields more than S16-F5, similar to S18-R6, S20-G7 and S20-M1and less than S21-C3 (LSD 0.05=4.6 bu/a). EE1600891 is similar inmaturity to S20-M1 and S21-C3 and later in maturity when compared toS18-R6, S20-G7, and S16-F5 (LSD 0.05=3.0). EE1600891 is higher inprotein content when compared to S18-R6, S20-G7, S20-M1, S16-F5, andS21-C3 (LSD 0.05=1.9). EE1600891 can be differentiated from S21-C3,S16-F5, and S20-M1 since EE1600891 has gray pubescence, tan pod wall,yellow hilum, and no genes for phytophthora resistance. S21-C3, S16-F5,and S20-M1 have gray pubescence, tan pod wall, yellow hilum, and theRps1c gene for phytophthora resistance. S18-R6 has gray pubescence, tanpod wall, yellow hilum, and the Rps1a gene for phytophthora resistance.S20-G7 has gray pubescence, brown pod wall, yellow hilum, and the Rps1cgene for phytophthora resistance.

EE1660258

EE1660258 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1660258 is a novel soybean cultivar with high yield potential andtolerance to Roundup™ herbicide using Roundup Ready 2 Yield® and Dicambaherbicide. The invention relates in part to seeds of the cultivarEE1660258, plants of the cultivar EE1660258 and to methods for producinga soybean plant produced by crossing the soybean cultivar EE1660258 byitself or to another soybean genotype.

EE1660258 is a Group 0 Maturity soybean cultivar. This variety has an RMof 0.700. To be sold commercially in Quebec and Ontario, Canada andareas of Minnesota and South Dakota where mid Group 0 maturity soybeansare grown. Specific area where best adaptation occurs includes: Quebec,and Ontario, Canada and Minnesota and South Dakota. The target for thisvariety is geographic areas that grow mid Group 0 maturity glyphosateand dicamba tolerant varieties where glyphosate resistant weeds existand require Soybean Cyst Nematode resistance.

The characteristics and traits of EE1660258 are listed below.

TABLE 7 CHARACTERISTICS AND TRAITS Herbicide Transgene MON 89788; MON87708 Insect Transgene Other Transgene Relative 0.700 MaturitySulfonylurea Tolerance N Seed Shape Hypocotyl Color Metribuzin ToleranceToler Seed Coat Luster Plant PLBG Morphological Aphid Gene Rag1_SPeroxidase Leaf Color % Protein @ 13% mst Seed Size g/100 seeds LeafShape Calculated % Oil @13% mst Growth Habit INDET Leaf Shape PlantHealth Phytophthora Gene Rps1c, Rps3a Stem Canker Tolerance Rust GeneChloride Sensitivity CLMS SCN Res 88788 RootKnot Nematode Sting NematodeSource R1 R2 R3 R5 R7 R9 R14 Incognita Arenaria Javanica Pratylenchus FI% FI % FI % FI % FI % FI % FI % SCN = Soybean Cyst Nematode, RKN = RootKnot Nematode Rps gene indicates the specific gene for resistance but ifnone are indicated then none are known to be present. % Protein and %Oil are given at 13% moisture (standard moisture). MON89788 indicatesthis variety carries the glyphosate tolerance transgene derived fromevent MON 89788; MON87708 indicates this variety carries the dicambatolerance transgene derived from event MON 87708. Seed shape: 1 =spherical; 2 = spherical-flattened; 3 = elongate; 4 = elongate-flattenedSeed coat luster: 1 = dull; 2 = shiny Plant Morphological traits arelisted in the order of flower, pubescence, pod color, and hilum. Forflower, P = purple, W = white, and S = segregating (mixture of colors).For pubescence, G = gray, T = tawny. Lt = LT = light tawny, LBr = LB =light brown, and S = segregating (mixture of colors). For pod color, T =tan, B = brown, LBr = light brown, and S = segregating (mixture ofcolors). For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF =Bf = buff, BL = Bl = black, IB = Ib = imperfect black, Y = yellow, IY =Iy = imperfect yellow, S = segregating (mixture of colors). Leaf Color:1 = light green; 2 = medium green; 3 = dark green Ratings are on a 1 to9 scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 8 Agronomic and Disease Traits Hrvst Grn Mat GS_ VHNO Yield EmergeLod Lod Days Height Canopy Branch R IDC S09-D4X 56.7 2.5 4.0 1.5 120.931.9 5.3 4.8 #N/A 4.0 AG06X8 53.5 2.7 3.0 6.5 118.0 34.6 5.3 5.5 #N/A2.0 S05-N5X 53.2 2.3 3.0 1.0 117.6 30.3 5.0 4.0 #N/A 3.9 S07-Q4X 53.22.7 2.0 1.0 118.9 31.1 5.2 5.0 #N/A 3.9 S06-Q9 53.2 2.4 3.0 1.0 116.831.1 5.0 5.5 #N/A 2.9 EE1660258 52.8 2.2 1.0 2.0 117.8 31.1 5.1 5.5 #N/A3.9 S06-K4X 51.6 2.9 3.0 1.0 118.4 31.5 5.8 6.0 #N/A 4.1 Environments18.0 5.0 1.0 1.0 8.0 1.0 5.0 2.0 #N/A 4.0 Grand 52.1 3.0 2.6 2.0 118.131.3 5.2 5.3 #N/A 3.9 Mean Check 51.3 3.0 2.8 1.9 117.6 31.5 5.2 5.4#N/A 3.7 Mean LSD (0.05) 2.6 0.7 0.0 2.8 1.3 0.0 0.6 1.2 #N/A 0.7 CR_PM_ BP_ SDS_ TSP_ VHNO BSR R FELSR R PRR R RUSTR R SWM R S09-D4X 1.0#N/A #N/A #N/A 2.5 #N/A #N/A #N/A 3.0 #N/A AG06X8 1.0 #N/A #N/A #N/A 3.0#N/A #N/A #N/A 4.8 #N/A S05-N5X 1.0 #N/A #N/A #N/A 2.5 #N/A #N/A #N/A3.6 #N/A S07-Q4X 2.0 #N/A #N/A #N/A 2.5 #N/A #N/A #N/A 3.3 #N/A S06-Q91.0 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 3.0 #N/A EE1660258 1.0 #N/A #N/A#N/A 2.5 #N/A #N/A #N/A 3.5 #N/A S06-K4X 1.0 #N/A #N/A #N/A 2.5 #N/A#N/A #N/A 5.0 #N/A Environments 1.0 #N/A #N/A #N/A 1.0 #N/A #N/A #N/A2.0 #N/A Grand 1.3 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 3.5 #N/A Mean Check1.3 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 4.0 #N/A Mean LSD (0.05) 1.3 #N/A#N/A #N/A 0.0 #N/A #N/A #N/A 1.7 #N/A

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1660258.EE1660258 yields similar to S06-K4X, S05-N5X, S07-Q4X, and S06-Q9 andless than S09-D4X (LSD 0.05=2.6 bu/a). EE1660258 is similar in maturityto S05-N5X, S06-09, S07-Q4X, and S06-K4X for maturity and earlier inmaturity when compared to S09-D4X (LSD 0.05=1.3). EE1660258 has similarIDC to S09-D4X, S05-N5X, S07-Q4X, and S06-K4X and worse than S06-Q9 (LSD0.05=0.7). EE1660258 has similar SWM to S09-D4X, S05-N5X, S07-Q4X, andS06-09 and better than S06-K4X (LSD 0.05=0.7). EE1660258 can bedifferentiated from S05-N5X since EE1660258 has light tawny pubescence,brown pod wall, grey hilum, the Rps1c and Rps3a genes for phytophthoraresistance, it contains the P188788 gene for soybean cyst nematoderesistance and the MON87708 gene for resistance to Dicamba. S05-N5X haslight tawny pubescence, tan pod wall, brown hilum, the Rps1c and Rps3agenes for phytophthora resistance, and does not contain the P188788 genefor soybean cyst nematode resistance and contains the MON87708 gene forDicamba resistance. S07-Q4X has light tawny pubescence, tan pod wall,black hilum, the Rps1c gene for phytophthora resistance, it contains theP188788 gene for soybean cyst nematode resistance and contains theMON87708 gene for Dicamba resistance. S09-D4X has light tawnypubescence, tan pod wall, brown hilum, the Rps1k and Rps3a genes forphytophthora resistance, and contains the P188788 gene for soybean cystnematode resistance and contains the MON87708 gene for Dicambaresistance. S06-Q9 has light tawny pubescence, tan pod wall, blackhilum, no genes for phytophthora resistance, and contains the P188788gene for soybean cyst nematode resistance and does not contain theMON87708 gene for Dicamba resistance. S06-K4X has light tawnypubescence, tan pod wall, black hilum, the Rps3a gene for phytophthoraresistance, and contains no gene for soybean cyst nematode resistanceand contains the MON87708 gene for Dicamba resistance.

EE1760174

EE1760174 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1760174 is a novel soybean cultivar with high yield potential andtolerance to Roundup™ herbicide using Roundup Ready 2 Yield® and Dicambaherbicide. The invention relates in part to seeds of the cultivarEE1760174, plants of the cultivar EE1760174 and to methods for producinga soybean plant produced by crossing the soybean cultivar EE1760174 byitself or to another soybean genotype.

EE1760174 is a Group 0 Maturity soybean cultivar. This variety has an RMof 0.700. To be sold commercially in Quebec and Ontario, Canada andareas of Minnesota and South Dakota where mid Group 0 maturity soybeansare grown. Specific area where best adaptation occurs includes: Quebec,and Ontario, Canada and Minnesota and South Dakota. The target for thisvariety is geographic areas that grow mid Group 0 maturity glyphosateand dicamba tolerant varieties where glyphosate resistant weeds existand require Soybean Cyst Nematode resistance.

The characteristics and traits of EE1760174 are listed below.

TABLE 9 CHARACTERISTICS AND TRAITS Herbicide Transgene MON 87708; MON89788 Insect Transgene Other Transgene Relative 0.700 MaturitySulfonylurea Tolerance N Seed Shape Hypocotyl Color Metribuzin ToleranceToler Seed Coat Luster Plant PTTBI Morphological Aphid Gene Rag1_SPeroxidase Leaf Color % Protein @ 13% mst Seed Size g/100 seeds LeafShape Calculated % Oil (@13% mst Growth Habit INDET Leaf Shape PlantHealth Phytophthora Gene S Stem Canker Tolerance Rust Gene ChlorideSensitivity CLMS SCN Res 88788 RootKnot Nematode Sting Nematode SourceR1 R2 R3 R5 R7 R9 R14 Incognita Arenaria Javanica Pratylenchus FI % FI %FI % FI % FI % FI % FI % MI_S SCN = Soybean Cyst Nematode, RKN = RootKnot Nematode Rps gene indicates the specific gene for resistance but ifnone are indicated then none are known to be present. % Protein and %Oil are given at 13% moisture (standard moisture). MON89788 indicatesthis variety carries the glyphosate tolerance transgene derived fromevent MON 89788; MON87708 indicates this variety carries the dicambatolerance transgene derived from event MON 87708. Seed shape: 1 =spherical; 2 = spherical-flattened; 3 = elongate; 4 = elongate-flattenedSeed coat luster: 1 = dull; 2 = shiny Plant Morphological traits arelisted in the order of flower, pubescence, pod color, and hilum. Forflower, P = purple, W = white, and S = segregating (mixture of colors).For pubescence, G = gray, T = tawny, Lt = LT = light tawny, LBr = LB =light brown, and S = segregating (mixture of colors). For pod color, T =tan, B= brown, LBr = light brown, and S = segregating (mixture ofcolors). For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF =Bf = buff, BL = Bl = black, IB-Ib= imperfect black, Y= yellow, IY = Iy =imperfect yellow, S = segregating (mixture of colors). Leaf Color: 1 =light green; 2 = medium green; 3 = dark green Ratings are on a 1 to 9scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 10 Agronomic and Disease Traits Hrvst Grn Mat GS_ VHNO YieldEmerge Lod Lod Days Height Canopy Branch R IDC S09-D4X 56.7 2.5 4.0 1.5120.9 31.9 5.3 4.8 #N/A 4.0 EE1760174 54.5 2.6 2.0 1.0 119.2 30.7 5.55.8 #N/A 3.8 AG06X8 53.5 2.7 3.0 6.5 118.0 34.6 5.3 5.5 #N/A 2.0 S05-NSX53.2 2.3 3.0 1.0 117.6 30.3 5.0 4.0 #N/A 3.9 S07-Q4X 53.2 2.7 2.0 1.0118.9 31.1 5.2 5.0 #N/A 3.9 S06-Q9 53.2 2.4 3.0 1.0 116.8 31.1 5.0 5.5#N/A 2.9 S06-K4X 51.6 2.9 3.0 1.5 118.4 31.5 5.8 6.0 #N/A 4.1Environments 18.0 5.0 1.0 1.0 8.0 1.0 5.0 2.0 #N/A 4.0 Grand 52.1 3.02.6 2.0 118.1 31.3 5.2 5.3 #N/A 3.9 Mean Check 51.3 3.0 2.8 1.9 117.631.5 5.2 5.4 #N/A 3.7 Mean LSD (0.05) 2.6 0.7 0.0 2.8 1.3 0.0 0.6 1.2#N/A 0.7 CR_ PM_ BP_ RUST SDS_ TSP_ VHNO BSR R FELSR R PRR R R R SWM RS09-D4X 1.0 #N/A #N/A #N/A 2.5 #N/A #N/A #N/A 3.0 #N/A EE1760174 2.0#N/A #N/A #N/A 3.0 #N/A #N/A #N/A 4.0 #N/A AG06X8 1.0 #N/A #N/A #N/A 3.0#N/A #N/A #N/A 4.8 #N/A S05-NSX 1.0 #N/A #N/A #N/A 2.5 #N/A #N/A #N/A3.6 #N/A S07-Q4X 2.0 #N/A #N/A #N/A 2.5 #N/A #N/A #N/A 3.3 #N/A S06-Q91.0 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 3.0 #N/A S06-K4X 1.0 #N/A #N/A#N/A 2.5 #N/A #N/A #N/A 5.0 #N/A Environments 1.0 #N/A #N/A #N/A 1.0#N/A #N/A #N/A 2.0 #N/A Grand 1.3 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 3.5#N/A Mean Check 1.3 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A 3.0 #N/A Mean LSD(0.05) 1.3 #N/A #N/A #N/A 0.0 #N/A #N/A #N/A 1.7 #N/A #N/A = no dataavailable

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1760174.EE1760174 yields similar to S09-D4X, S05-N5X, S07-04X, and S06-09 andmore than S06-K4X (LSD 0.05=2.6 bu/a). EE1760174 is later in maturitythan S05-N5X and S06-09 and similar in maturity to S07-04X, and S06-K4Xfor maturity and earlier in maturity when compared to S09-D4X (LSD0.05-1.3). EE1760174 has similar IDC to S09-D4X, S05-N5X, S07-Q4X, andS06-K4X and worse than S06-Q9 (LSD 0.05=0.7). EE1760174 can bedifferentiated from S07-Q4X since EE1760174 has tawny pubescence, tanpod wall, black hilum, no gene for phytophthora resistance, it containsthe P188788 gene for soybean cyst nematode resistance and the MON87708gene for resistance to Dicamba. S07-Q4X has light tawny pubescence, tanpod wall, black hilum, the Rps1c gene for phytophthora resistance, itcontains the P188788 gene for soybean cyst nematode resistance andcontains the MON87708 gene for Dicamba resistance. S05-N5X has lighttawny pubescence, tan pod wall, brown hilum, the Rps1c and Rps3a genesfor phytophthora resistance, and does not contain the P188788 gene forsoybean cyst nematode resistance and contains the MON87708 gene forDicamba resistance. S09-D4X has light tawny pubescence, tan pod wall,brown hilum, the Rps1k and Rps3a genes for phytophthora resistance, andcontains the P188788 gene for soybean cyst nematode resistance andcontains the MON87708 gene for Dicamba resistance.

S06-09 has light tawny pubescence, tan pod wall, black hilum, no genesfor phytophthora resistance, and contains the P188788 gene for soybeancyst nematode resistance and does not contain the MON87708 gene forDicamba resistance. S06-K4X has light tawny pubescence, tan pod wall,black hilum, the Rps3a gene for phytophthora resistance, and contains nogene for soybean cyst nematode resistance and contains the MON87708 genefor Dicamba resistance.

EE1760847

EE1760847 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1760847 is a novel soybean cultivar with high yield potential andtolerance to Roundup Tm herbicide using Roundup Ready 2 Yield® andDicamba herbicide. The invention relates in part to seeds of thecultivar EE1760847, plants of the cultivar EE1760847 and to methods forproducing a soybean plant produced by crossing the soybean cultivarEE1760847 by itself or to another soybean genotype.

EE1760847 is a Group 0 Maturity soybean cultivar. This variety has an RMof 0.500. To be sold commercially in Quebec and Ontario, Canada andareas of Minnesota and South Dakota where mid Group 0 maturity soybeansare grown. Specific area where best adaptation occurs includes: Quebec,and Ontario, Canada and Minnesota and South Dakota. The target for thisvariety is geographic areas that grow mid Group 0 maturity glyphosateand dicamba tolerant varieties where glyphosate resistant weeds existand require Soybean Cyst Nematode resistance.

The characteristics and traits of EE1760847 are listed below.

TABLE 11 CHARACTERISTICS AND TRAITS Herbicide Transgene MON 87708; MON89788 Insect Transgene Other Transgene Relative 0.500 MaturitySulfonylurea Tolerance N Seed Shape Hypocotyl Color Metribuzin ToleranceToler Seed Coat Luster Plant PLTBI Morphological Aphid Gene Rag1_SPeroxidase Leaf Color % Protein @ 13% mst Seed Size g/100 seeds LeafShape Calculated % Oil @13% mst Growth Habit INDET Leaf Shape PlantHealth Phytophthora Gene S Stem Canker Tolerance Rust Gene ChlorideSensitivity CLMS SCN Res RootKnot Nematode Sting Source 88788 NematodeR1 R2 R3 R5 R7 R9 R14 Incognita Arenaria Javanica Pratylenchus FI % FI %FI % FI % FI % FI % FI % MI_X SCN = Soybean Cyst Nematode, RKN = RootKnot Nematode Rps gene indicates the specific gene for resistance but ifnone are indicated then none are known to be present. % Protein and %Oil are given at 13% moisture (standard moisture). MON89788 indicatesthis variety carries the glyphosate tolerance transgene derived fromevent MON 89788; MON87708 indicates this variety carries the dicambatolerance transgene derived from event MON 87708. Seed shape: 1 =spherical; 2 = spherical-flattened; 3 = elongate; 4 = elongate-flattenedSeed coat luster: 1 = dull; 2 = shiny Plant Morphological traits arelisted in the order of flower, pubescence, pod color, and hilum. Forflower, P = purple, W = white, and S = segregating (mixture of colors).For pubescence, G = gray, T = tawny, Lt = LT = light tawny, LBr = LB =light brown, and S = segregating (mixture of colors). For pod color, T =tan, B = brown, LBr = light brown, and S = segregating (mixture ofcolors). For hilum, G = gray, BR = Br = brown, MBr = medium brown, BF =Bf = buff, BL = Bl = black, IB = Ib = imperfect black, Y = yellow, IY =Iy = imperfect yellow, S = segregating (mixture of colors). Leaf Color:1 = light green; 2 = medium green; 3 = dark green Ratings are on a 1 to9 scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine, MI_X = trait is segregating for susceptible andresistant plants, it is not fixed

TABLE 12 Agronomic and Disease Traits Hrvst Grn Mat GS_ VHNO YieldEmerge Lod Lod Days Height Canopy Brand R IDC S05-NSX 51.5 2.9 3.0 1.5117.3 28.3 5.0 3.2 #N/A 4.2 EE1760847 51.4 2.0 2.3 1.5 116.6 28.5 4.64.0 #N/A 3.2 S02-F9X 47.3 3.0 2.0 1.5 112.1 28.7 4.3 4.3 #N/A 4.6 S03-G950.4 2.9 4.3 3.5 114.7 28.3 4.5 5.5 #N/A 2.8 S01-C4X 46.4 2.9 4.0 2.0111.8 30.5 4.7 4.7 #N/A 4.5 AG03X7 48.1 3.1 3.3 5.0 114.7 27.2 5.0 3.8#N/A 2.6 AG04X9 47.3 3.0 3.5 3.5 114.1 35.0 5.6 3.8 #N/A 3.3Environments 22.0 5.0 2.0 1.0 9.0 1.0 7.0 3.0 #N/A 4.0 Grand 48.1 3.13.3 2.1 114.5 28.7 4.9 4.9 #N/A 3.7 Mean Check 46.6 3.2 3.5 2.8 113.629.5 4.7 4.6 #N/A 3,3 Mean LSD (0.05) 2.1 0.7 1.3 0.0 1.1 2.3 0.5 1.4#N/A 0.7 CR_ PM_ BP_ SDS_ SCL_ TSP_ VHNO BSR R FELSR R PRR R RUSTR R R RS05-NSX 1.0 #N/A #N/A #N/A 3.5 #N/A #N/A #N/A #N/A #N/A EE1760847 1.0#N/A #N/A #N/A 3.5 #N/A #N/A #N/A #N/A #N/A S02-F9X 2.0 #N/A #N/A #N/A3.0 #N/A #N/A #N/A #N/A #N/A S03-G9 1.0 #N/A #N/A #N/A 3.5 #N/A #N/A#NIA #N/A #N/A S01-C4X 3.0 #N/A #N/A #N/A 4.0 #N/A #N/A #N/A #N/A #N/AAG03X7 2.5 #N/A #N/A #N/A 3.5 #N/A #N/A #N/A #N/A #N/A AG04X9 1.0 #N/A#N/A #N/A 5.5 #N/A #N/A #N/A #N/A #N/A Environments 1.0 #N/A #N/A #N/A1.0 #N/A #N/A #N/A #N/A #N/A Grand 1.5 #N/A #N/A #N/A 4.0 #N/A #N/A #N/A#N/A #N/A Mean Check 1.5 #N/A #N/A #N/A 3.9 #N/A #N/A #N/A #N/A #N/AMean LSD (0.05) 1.6 #N/A #N/A #N/A 2.1 #N/A #N/A #N/A #N/A #N/A #N/A =no data available

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1760847.EE1760847 yields similar to S05-N5X and S03-G9 and more than S02-F9X andS01-C4X (LSD 0.05=2.1 bu/a). EE1760847 is later in maturity thanS01-C4X, S03-G9 and S02-F9X and similar in maturity to S05-N5X formaturity (LSD 0.05=1.1). EE1760847 has similar IDC to S03-G9 and betterthan S05-N5X, S02-F9X, and S01-C4X (LSD 0.05=0.7). EE1760847 has similarharvest lodging to S05-N5X and S02-F9X and better than S03-G9 andS01-C4X (LSD 0.05=1.3). EE1760847 can be differentiated from S03-G9since EE1760847 has light tawny pubescence, tan pod wall, black hilum,no gene for phytophthora resistance, it contains the P188788 gene forsoybean cyst nematode resistance and the MON87708 gene for resistance toDicamba. S03-G9 has light tawny pubescence, tan pod wall, black hilum,no gene for phytophthora resistance, it contains the P188788 gene forsoybean cyst nematode resistance but does not contain the MON87708 genefor Dicamba resistance. S02-F9X has grey pubescence, tan pod wall, buffhilum, the Rps1c gene for phytophthora resistance, and does not containthe P188788 gene for soybean cyst nematode resistance and contains theMON87708 gene for Dicamba resistance. S01-C4X has light tawnypubescence, tan pod wall, black hilum, the Rps1c gene for phytophthoraresistance, does not contain the P188788 gene for soybean cyst nematoderesistance and contains the MON87708 gene for Dicamba resistance.

EE1761104

EE1761104 is employed in a number of plot repetitions to establish traitcharacteristics.

EE1761104 is a novel soybean cultivar with high yield potential andtolerance to Roundup Tm herbicide using Roundup Ready 2 Yield® andDicamba herbicide. The invention relates to seeds of the cultivarEE1761104, plants of the cultivar EE1761104 and to methods for producinga soybean plant produced by crossing the soybean cultivar EE1761104 byitself or to another soybean genotype.

EE1761104 is a Group 0 Maturity soybean cultivar. This variety has an RMof 0.400. To be sold commercially in Quebec and Ontario, Canada andareas of Minnesota and South Dakota where mid Group 0 maturity soybeansare grown. Specific area where best adaptation occurs includes: Quebec,and Ontario, Canada and Minnesota and South Dakota. The target for thisvariety is geographic areas that grow mid Group 0 maturity glyphosateand dicamba tolerant varieties where glyphosate resistant weeds existand require Soybean Cyst Nematode resistance.

The characteristics and traits of EE1761104 are listed below.

TABLE 13 CHARACTERISTICS AND TRAITS Herbicide Transgene MON 87708; MON89788 Insect Transgene Other Transgene Relative 0.400 MaturitySulfonylurea Seed Shape Hypocotyl Tolerance Color Metribuzin Toler SeedCoat Luster Plant PLTBI Tolerance Morphological Aphid Gene Rag1_SPeroxidase Leaf Color % Protein @ 13% mst Seed Size g/100 seeds LeafShape Calculated % Oil @13% mst Growth Habit INDET Leaf Shape PlantHealth Phytophthora Gene Stem Canker Tolerance Rust Gene ChlorideSensitivity CLMS SCN Res 88788 RootKnot Nematode Sting Nematode SourceR1 R2 R3 R5 R7 R9 R14 Incognita Arenaria Javanica Pratylenchus FI % FI %FI % FI % FI % FI % FI % MI_U SCN = Soybean Cyst Nematode, RKN = RootKnot Nematode Rps gene indicates the specific gene for resistance but ifnone are indicated then none are known to be present. % Protein and %Oll are given at 13% moisture (standard moisture) MON89788 indicatesthis variety carries the glyphosate tolerance transgene derived fromevent MON 89788; MON87708 indicates this variety carries the dicambatolerance transgene derived from event MON 87708. Seed shape: 1 =spherical; 2 = spherical-flattened; 3 = elongate; 4 = elongate-flattenedSeed coat luster: 1 = dull; 2 = shiny Plant Morphological traits arelisted in the order of flower, pubescence, pod color, and hilum. Forflower. P = purple, W = white, and S = segregating (mixture of colors).For pubescence, G = gray, T = tawny, Lt = LT = light tawny, LBr = LB =light brown, and S = segregating (mixture of colors). For pod color, T =tan, B = brown, LBr = light brown, and S= segregating (mixture ofcolors). For hilum, G = gray. BR = Br = brown, MBr = medium brown, BF =Bf = buff, BL-Bl = black, IB = Ib = imperfect black, Y = yellow, IY = Iy= imperfect yellow, S = segregating (mixture of colors). Leaf Color: 1 =light green; 2 = medium green; 3 = dark green Ratings are on a 1 to 9scale with 1 being the best. Sting Nematode is Pratylenchus. Chloridesensitivity: CL = chloride, M = molecular marker results, X =segregating, S = susceptible marker allele present, R = resistant markerallele present. CLMS = chloride sensitive and CLMR = chloride resistantMI_S = susceptible, MI_R = resistant, MI_MR = mixed resistance. MI_U =unable to determine

TABLE 14 Agronomic and Disease Traits Hrvst Grn Mat GS_ VHNO YieldEmerge Lod Lod Days Height Canopy Branch R IDC EE1761104 51.7 3.2 2.51.0 115.6 28.5 4.9 5.0 #N/A 3.3 S05-NSX 51.5 2.9 3.0 1.5 117.3 28.3 5.04.2 #N/A 4.2 S02-F9X 47.3 3.0 2.0 1.5 112.1 28.7 4.3 4.3 #N/A 4.6 S03-G950.4 2.9 4.3 3.5 114.7 28.3 4.5 5.5 #N/A 2.8 S01-C4X 46.4 2.9 4.0 2.0111.8 30.5 4.7 4.7 #N/A 4.5 AG03X7 48.1 3.1 3.3 5.0 114.7 27.2 5.0 3.8#N/A 2.6 AG04X9 47.3 3.0 3.5 3.5 114.1 35.0 5.6 3.8 #N/A 3.3Environments 22.0 5.0 2.0 1.0 9.0 1.0 7.0 3.0 #N/A 4.0 Grand 48.1 3.13.3 2.1 114.5 28.7 4.9 4.9 #N/A 3.7 Mean Check 46.6 3.2 3.5 2.6 113.629.5 4.7 4.6 #N/A 3.3 Mean LSD (0.05) 2.1 0.7 1.3 0.0 1.1 2.3 0.5 1.4#N/A 0.7 CR_ PM_ BP_ SDS_ SCL_ TSP_ VHNO BSR R FELSR R PRR R RUSTR R R REE1761104 1.0 #N/A #N/A #N/A 3.0 #N/A #N/A #N/A #N/A #N/A S05-NSX 1.0#N/A #N/A #N/A 3.5 #N/A #N/A #N/A #N/A #N/A S02-F9X 2.0 #N/A #N/A #N/A3.0 #N/A #N/A #N/A #N/A #N/A S03-G9 1.0 #N/A #N/A #N/A 3.5 #N/A #N/A#N/A #N/A #N/A S01-C4X 3.0 #N/A #N/A #N/A 4.0 #N/A #N/A #N/A #N/A #N/AAG03X7 2.5 #N/A #N/A #N/A 3.5 #N/A #N/A #N/A #N/A #N/A AG04X9 1.0 #N/A#N/A #N/A 5.5 #N/A #N/A #N/A #N/A #N/A Environments 1.0 #N/A #N/A #N/A1.0 #N/A #N/A #N/A #N/A #N/A Grand 1.5 #N/A #N/A #N/A 4.0 #N/A #N/A #N/A#N/A #N/A Mean Check 1.5 #N/A #N/A AN/A 3.9 #N/A #N/A #N/A #N/A #N/AMean LSD (0.05) 1.6 #N/A #N/A #N/A 2.1 #N/A #N/A #N/A #N/A #N/A #N/A =no data available

As the previous table indicates each of these lines has their ownpositive traits. Each of these lines is different from EE1761104.EE1761104 yields similar to S05-N5X and S03-G9 and more than S02-F9X andS01-C4X (LSD 0.05=2.1 bu/a). EE1761104 is later in maturity than S01-C4Xand S02-F9X and similar in maturity to S03-G9 and earlier than S05-N5Xfor maturity (LSD 0.05=1.1). EE1761104 has similar IDC to S03-G9 andbetter than S05-N5X, S02-F9X, and S01-C4X (LSD 0.05=0.7). EE1761104 hassimilar harvest lodging to S05-N5X and S02-F9X and better than S03-G9and S01-C4X (LSD 0.05=1.3). EE1761104 can be differentiated from S03-G9since EE1761104 has light tawny pubescence, tan pod wall, black hilum,no gene for phytophthora resistance, it contains the P188788 gene forsoybean cyst nematode resistance and the MON87708 gene for resistance toDicamba. S03-G9 has light tawny pubescence, tan pod wall, black hilum,no gene for phytophthora resistance, it contains the P188788 gene forsoybean cyst nematode resistance but does not contain the MON87708 genefor Dicamba resistance. S02-F9X has grey pubescence, tan pod wall, buffhilum, the Rps1c gene for phytophthora resistance, and does not containthe P188788 gene for soybean cyst nematode resistance and contains theMON87708 gene for Dicamba resistance. S01-C4X has light tawnypubescence, tan pod wall, black hilum, the Rps1c gene for phytophthoraresistance, does not contain the P188788 gene for soybean cyst nematoderesistance and contains the MON87708 gene for Dicamba resistance.

Accordingly, the present invention has been described with some degreeof particularity directed to the preferred embodiment of the presentinvention. It should be appreciated, though that the present inventionis defined by the following claims construed in light of the prior artso that modifications or changes may be made to the preferred embodimentof the present invention without departing from the inventive conceptscontained herein.

1. A plant, a plant part, or a seed of soybean variety EE1761104,wherein a representative sample of seed of said soybean varietyEE1761104 has been deposited under ATCC Accession Number.
 2. A cell ofthe plant of claim
 1. 3. A soybean plant obtained by transforming thesoybean plant of claim
 1. 4. A seed of the soybean plant according toclaim
 3. 5. A method for producing a soybean seed, said methodcomprising crossing soybean plants and harvesting the resultant soybeanseed, wherein at least one soybean plant is the soybean plant ofclaim
 1. 6. The method of claim 5, wherein the method further comprises:(a) crossing a plant grown from said resultant soybean seed with itselfor a different soybean plant to produce a seed of a progeny plant of asubsequent generation; (b) growing a progeny plant of a subsequentgeneration from said seed of a progeny plant of a subsequent generationand crossing the progeny plant of a subsequent generation with itself ora second plant to produce a progeny plant of a further subsequentgeneration; and (c) repeating steps (a) and (b) using said progeny plantof a further subsequent generation from step (b) in place of the plantgrown from said resultant soybean seed in step (a), wherein steps (a)and (b) are repeated with sufficient inbreeding to produce an inbredsoybean plant derived from soybean variety EE1761104.
 7. An F1 soybeanseed produced by the method of claim
 5. 8. An F1 soybean seed producedby the method of claim 5 wherein at least one of the soybean plantscarries a heritable transgenic event.
 9. An F1 soybean plant, or partthereof, produced by growing said seed of claim
 7. 10. A method fordeveloping a second soybean plant through plant breeding, said methodcomprising applying plant breeding to said soybean plant, or partsthereof according to claim 1, wherein said plant breeding results indevelopment of said second soybean plant.
 11. A method of producing asoybean plant comprising a desired trait, the method comprisingintroducing at least one transgene or locus conferring the desired traitinto the soybean plant EE1761104 of claim
 1. 12. The method of claim 11,wherein the desired trait is selected from the group consisting of malesterility, herbicide tolerance, insect resistance, nematode resistance,pest resistance, disease resistance, fungal resistance, modified fattyacid metabolism, modified carbohydrate metabolism, drought tolerance,abiotic stress tolerance, a site-specific recombination site, andmodified nutrient deficiency tolerances.
 13. A plant produced by themethod of claim 11, wherein the plant has said desired trait and all ofthe morphological and physiological characteristics of soybean varietyEE1761104 other than those characteristics altered by said transgene orlocus when grown in the same location and in the same environment.
 14. Amethod of introducing a single locus conversion into a soybean plant,wherein the method comprises: (a) crossing the EE1761104 plant of claim1 with a plant of another soybean variety that comprises the singlelocus to produce F1 progeny plants; (b) selecting one or more F1 progenyplants from step (a) to produce selected progeny plants; (c) selfingselected progeny plants of step (b) or crossing the selected progenyplants of step (b) with the EE1761104 plants to produce later generationselected progeny plants; (d) crossing or further selecting for latergeneration selected progeny plants that have the single locus andphysiological and morphological characteristics of soybean varietyEE1761104 to produce selected next later generation progeny plants; andoptionally (e) repeating crossing or selection of later generationprogeny plants to produce progeny plants that comprise the single locusand all of the physiological and morphological characteristics of saidsingle locus and of soybean variety EE1761104 when grown in the samelocation and in the same environment.
 15. A plant produced by the methodof claim 14 or a selfed progeny thereof, wherein the plant or selfedprogeny thereof comprises said single locus and otherwise comprisesessentially all of the physiological and morphological characteristicsof soybean variety EE1761104.
 16. A method of producing a commodityplant product, said method comprising obtaining the plant of claim 1 ora part thereof and producing said commodity plant product comprisingprotein concentrate, protein isolate, soybean hulls, meal, flour, or oilfrom said plant or said part thereof.
 17. A seed that produces the plantof claim
 13. 18. A method comprising isolating nucleic acids from aplant, a plant part, or a seed of soybean variety EE1761104, analyzingsaid nucleic acids to produce data, and recording the data for soybeanvariety EE1761104.
 19. The method of claim 18, wherein the data isrecorded on a computer readable medium.
 20. The method of claim 18,further comprising using the data for crossing, selection, oradvancement decisions in a breeding program.